UNDA 8 (HAMAMELIS VIRGINIANA, MILLEFOLIUM, EQUISETUM ARVENSE, MERCURIALIS PERENNIS, THLASPI BURSA-PASTORIS, CACTUS GRANDIFLORUS, CRATAEGUS, CUPRUM METALLICUM) LIQUID UNDA 5 (TORMENTILLA, TUSS

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  • UNDA 8 (HAMAMELIS VIRGINIANA, MILLEFOLIUM, EQUISETUM ARVENSE, MERCURIALIS PERENNIS, THLASPI BURSA-PASTORIS, CACTUS GRANDIFLORUS, CRATAEGUS, CUPRUM METALLICUM) LIQUID UNDA 5 (TORMENTILLA, TUSS

UNDA 8 (HAMAMELIS VIRGINIANA, MILLEFOLIUM, EQUISETUM ARVENSE, MERCURIALIS PERENNIS, THLASPI BURSA-PASTORIS, CACTUS GRANDIFLORUS, CRATAEGUS, CUPRUM METALLICUM) LIQUID UNDA 5 (TORMENTILLA, TUSS
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NDC 62106-1104-8, 62106-1107-8, 62106-1113-8, 62106-1155-8, 62106-1158-8, 62106-1165-8
Set ID 1789ed21-3bc9-3b86-e054-00144ff88e88
Category HUMAN OTC DRUG LABEL
Packager Seroyal USA
Generic Name
Product Class
Product Number
Application Number
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  • ACTIVE INGREDIENT

    Active ingredients

    Each drop contains:

    Tormentilla (Bloodwort) Rhizome . 4X
    Tussilago farfara (Coltsfoot) Whole Plant . 4X
    Adiantum capillus-veneris (Maidenhair) Leaf. 4X
    Glycyrrhiza glabra (Licorice) Root . 4X
    Drosera (Sundew)Whole Plant . 4X
    Grindelia Aerial Parts. 4X
    Inula helenium (Elecampane) Root . 4X
    Cuprum metallicum(Copper) . 12X
    Argentum metallicum(Silver). 12X

  • PURPOSE

    Uses

    For the temporary relief of symptoms
    associated with common colds.

  • WARNINGS

    Warnings

    Sore throat warning: Severe or persistent sore throat or sore throat accompanied by high fever, headache,
    nausea and vomiting may be serious.
    Consult physician promptly. Do not use more than 2 days or administer to children under 3 years of age unless directed by physician.

    Ask a doctor before use if you have Persistent or chronic cough such as occurs with smoking, asthma, chronic
    bronchitis, or emphysema. Cough that is accompanied by excessive phlegm (mucus) or fever.

    Stop use and ask a doctor if Cough persists for more than 1 week, tends to recur, or is accompanied by a
    fever, rash, or persistent headache. A persistent cough may be a sign of a serious condition.
    And if symptoms persist or worsen.

    If pregnant or breastfeeding, ask a health professional before use.
    Keep out of reach of children.

    In case of overdose, get medical help or contact a Poison Control Center right away.

  • PREGNANCY OR BREAST FEEDING

    If you are pregnant or breastfeeding, ask a healthcare practitioner before use.

  • KEEP OUT OF REACH OF CHILDREN

    Keep out of reach of children.

  • OVERDOSAGE

    In case of overdose, get medical help or contact a Poison Control Center right away.

  • INACTIVE INGREDIENT

    Inactive Ingredients:

    Ethanol (beet),
    purified water

  • DOSAGE & ADMINISTRATION

    Directions

    Adults and adolescents (12 years and older)

    Take 5 drops three times daily or as recommended by your healthcare practitioner.

    Children (under 12 years)

    Take under the direction of your healthcare practitioner.

  • INDICATIONS & USAGE

    Uses

    For the temporary relief of symptoms associated with common colds.

    Directions

    Adults and adolescents (12 years and older)

    Take 5 drops three times daily or as recommended by your healthcare practitioner.

    Children (under 12 years)

    Take under the direction of your healthcare practitioner.

  • ACTIVE INGREDIENT

    Active ingredients

    Each drop contains:
    Cactus grandiflorus (Night-blooming cereus) Stem and Flower 4X
    Crataegus (Hawthorn) Fruit 4X
    Cuprum metallicum (Copper) 12X
    Equisetum arvense (Common horsetail) Stem 4X
    Hamamelis virginiana (Witch hazel) Bark 4X
    Mercurialis perennis (Dog's mercury) Whole Plant 4X
    Millefolium (Yarrow) Aerial Parts 4X
    Thlaspi bursa-pastoris (Shepherd’s purse) Aerial Parts 4X

  • PURPOSE

    Uses
    For the temporary relief of symptoms associated with overall poor circulation.

  • WARNINGS

    Warnings
    Stop use and ask a doctor if symptoms
    persist or worsen.
    If pregnant or breastfeeding, ask a
    health professional before use.
    Keep out of reach of children. In case
    of overdose, get medical help or contact
    a Poison Control Center right away.

  • PREGNANCY OR BREAST FEEDING

    If pregnant or breastfeeding, ask a health professional before use.

  • KEEP OUT OF REACH OF CHILDREN

    Keep out of reach of children.

  • OVERDOSAGE

    In case of overdose, get medical help or contact a Poison Control Center right away.

  • STOP USE

    Stop use and ask a doctor if symptoms persist or worsen

  • INACTIVE INGREDIENT

    Inactive Ingredients:

    Ethanol (beet),
    purified water

  • DOSAGE & ADMINISTRATION

    Directions

    Adults and adolescents (12 years and older)

    Take 5 drops three times daily or as recommended by your healthcare practitioner.

    Children (under 12 years)

    Take under the direction of your healthcare practitioner.

  • INDICATIONS & USAGE

    Uses
    For the temporary relief of symptoms associated with overall poor circulation.

    Directions

    Adults and adolescents (12 years and older)

    Take 5 drops three times daily or as recommended by your healthcare practitioner.

    Children (under 12 years)

    Take under the direction of your healthcare practitioner.

  • OTHER SAFETY INFORMATION

    Other information
    Do not use if seal is missing or broken.
    Store in a cool, dry place.

  • ACTIVE INGREDIENT

    Active ingredients
    Each drop contains:
    Argentum metallicum (Silver) 12X
    Aurum metallicum (Gold) 12X
    Camphora (Camphor from
    Cinnamomum camphora) 4X
    Cuprum metallicum (Copper) 12X
    Eucalyptus globulus (Fever tree) Leaf 4X
    Inula helenium (Elecampane) Root 4X
    Jateorhiza palmata (Columbo) Root 4X

  • PURPOSE

    Uses
    For the temporary relief of symptoms
    associated with low energy and common colds

  • WARNINGS

    Warnings
    Ask a doctor before use if you have
    Persistent or chronic cough such as
    occurs with smoking, asthma, chronic
    bronchitis, or emphysema.

    Cough that is accompanied by
    excessive phlegm (mucus) or fever.
    Stop use and ask a doctor if
    Cough persists for more than 1 week,
    tends to recur, or is accompanied by a
    fever, rash, or persistent headache. A
    persistent cough may be a sign of a
    serious condition.
    Symptoms persist or worsen.
    If pregnant or breastfeeding, ask a
    health professional before use.
    Keep out of reach of children. In case
    of overdose, get medical help or contact
    a Poison Control Center right away.

  • PREGNANCY OR BREAST FEEDING

    If you are pregnant or breastfeeding, ask a healthcare practitioner before use.

  • KEEP OUT OF REACH OF CHILDREN

    Keep out of reach of children.

  • OVERDOSAGE

    In case of overdose, get medical help or contact a Poison Control Center right away.

  • STOP USE

    Stop use and ask a doctor if
    Cough persists for more than 1 week,
    tends to recur, or is accompanied by a
    fever, rash, or persistent headache. A
    persistent cough may be a sign of a
    serious condition.
    Symptoms persist or worsen.

  • INACTIVE INGREDIENT

    Inactive Ingredients:

    Ethanol (beet),
    purified water

  • DOSAGE & ADMINISTRATION

    Directions

    Adults and adolescents (12 years and older): Take 5 drops three times daily or as
    recommended by your healthcare practitioner.
    Children (under 12 years): Take under the direction of your
    healthcare practitioner.

  • INDICATIONS & USAGE

    Uses
    For the temporary relief of symptoms
    associated with low energy and common colds

    Directions
    Adults and adolescents (12 years and older): Take 5 drops three times daily or as
    recommended by your healthcare practitioner.
    Children (under 12 years): Take under the direction of your
    healthcare practitioner.

  • OTHER SAFETY INFORMATION

    Other information
    Do not use if seal is missing or broken.
    Store in a cool, dry place.

  • ACTIVE INGREDIENT

    Active ingredients

    Each drop contains:

    Menyanthes trifoliata (Buckbean) Whole Plant . 4X
    Viola tricolor (Pansy) Whole Plant. 4X
    Hydrastis canadensis (Golden seal) Rhizome and Root . 10X
    Aloe socotrina (Aloes) Inspissated Juice. 10X

  • PURPOSE

    Indications
    For the relief of symptoms associated with anxiousness.

  • WARNINGS

    Warnings
    If you are pregnant or breastfeeding, ask a healthcare practitioner before use.
    Keep out of reach of children.
    In case of overdose, get medical help or contact a Poison Control Center right away.
    If symptoms persist or worsen, consult your healthcare practitioner.

  • PREGNANCY OR BREAST FEEDING

    If you are pregnant or breastfeeding, ask a healthcare practitioner before use.

  • KEEP OUT OF REACH OF CHILDREN

    Keep out of reach of children.

  • OVERDOSAGE

    In case of overdose, get medical help or contact a Poison Control Center right away.

  • ASK DOCTOR

    If symptoms persist or worsen, consult your healthcare practitioner.

  • INACTIVE INGREDIENT

    Inactive Ingredients:

    Ethanol (beet),
    purified water

  • DOSAGE & ADMINISTRATION

    Directions

    Adults and adolescents (12 years and older)

    Take 5 drops three times daily or as recommended by your healthcare practitioner.

    Children (under 12 years)

    Take under the direction of your healthcare practitioner.

  • INDICATIONS & USAGE

    Indications
    For the relief of symptoms associated with anxiousness.

    Directions

    Adults and adolescents (12 years and older)

    Take 5 drops three times daily or as recommended by your healthcare practitioner.

    Children (under 12 years)

    Take under the direction of your healthcare practitioner.

  • ACTIVE INGREDIENT

    Active ingredients
    Each drop contains:
    Aloe Inspissated Juice 6X
    Berberis vulgaris (Barberry) Bark 6X
    Boldo Leaf 6X
    Chelidonium majus (Greater celandine) Root and Rhizome 6X
    Juniperus communis (Common juniper) Berry 6X
    Urtica dioica (Common nettle) Whole Plant 6X

  • PURPOSE

    Uses

    For the temporary relief of symptoms associated with poor digestion and lack of appetite.

  • WARNINGS

    Warnings
    Stop use and ask a doctor if symptoms
    persist or worsen.

    If pregnant or breastfeeding, ask a
    health professional before use.
    Keep out of reach of children. In case
    of overdose, get medical help or contact
    a Poison Control Center right away.

  • PREGNANCY OR BREAST FEEDING

    If you are pregnant or breastfeeding, ask a healthcare practitioner before use.

  • KEEP OUT OF REACH OF CHILDREN

    Keep out of reach of children.

  • OVERDOSAGE

    In case of overdose, get medical help or contact a Poison Control Center right away.

  • STOP USE

    Stop use and ask a doctor If symptoms persist or worsen.

  • INACTIVE INGREDIENT

    Inactive Ingredients:

    Ethanol (beet),
    purified water

  • DOSAGE & ADMINISTRATION

    Directions
    Adults and adolescents (12 years and older): Take 5 drops three times daily or as
    recommended by your healthcare practitioner.
    Children (under 12 years): Take under the direction of your
    healthcare practitioner.

  • INDICATIONS & USAGE

    Uses
    For the temporary relief of symptoms associated with poor digestion and lack of appetite.

    Directions
    Adults and adolescents (12 years and older): Take 5 drops three times daily or as
    recommended by your healthcare practitioner.
    Children (under 12 years): Take under the direction of your
    healthcare practitioner.

  • OTHER SAFETY INFORMATION

    Other information
    Do not use if seal is missing or broken.
    Store in a cool, dry place.

  • ACTIVE INGREDIENT

    Active ingredients
    Each drop contains:
    Berberis vulgaris (Barberry) Bark 4X
    Boldo Leaf 4X
    Bryonia dioica (Bryony) Root 4X
    Hydrastis canadensis (Goldenseal) Rhizome and Root 4X
    Lycopodium clavatum (Clubmoss) Spore 4X
    Mercurialis annua Aerial Parts 4X
    Solidago virgaurea (Goldenrod) Inflorescences 4X

  • PURPOSE

    Uses
    For the temporary relief of symptoms associated with
    poor digestion
    minor urinary discomfort

  • WARNINGS

    Warnings

    Stop use and ask a doctor if symptoms persist or worsen.

    If you are pregnant or breastfeeding, ask a healthcare practitioner before use.
    Keep out of reach of children.
    In case of overdose, get medical help or contact a Poison Control Center right away.

  • PREGNANCY OR BREAST FEEDING

    If you are pregnant or breastfeeding, ask a healthcare practitioner before use.

  • KEEP OUT OF REACH OF CHILDREN

    Keep out of reach of children.

  • OVERDOSAGE

    In case of overdose, get medical help or contact a Poison Control Center right away.

  • INACTIVE INGREDIENT

    Inactive Ingredients:

    Ethanol (beet),
    purified water

  • DOSAGE & ADMINISTRATION

    Directions
    Adults and adolescents (12 years and older)

    Take 5 drops three times daily or as recommended by your healthcare practitioner.

    Children (under 12 years)

    Take under the direction of your healthcare practitioner.

  • INDICATIONS & USAGE

    Uses
    For the temporary relief of symptoms associated with
    poor digestion
    minor urinary discomfort

    Directions
    Adults and adolescents (12 years and older)

    Take 5 drops three times daily or as recommended by your healthcare practitioner.

    Children (under 12 years)

    Take under the direction of your healthcare practitioner.

  • OTHER SAFETY INFORMATION

    Other information
    Do not use if seal is missing or broken.
    Store in a cool, dry place.
    Contents may not fill package in order
    to accommodate required labeling.
    Please rely on stated quantity.

  • PRINCIPAL DISPLAY PANEL

    62106-1165-8

    NDC 62106-1165-8

    UNDA

    numbered compounds

    UNDA 258

    Homeopathic Preparation

    For the temporary relief of symptoms associated with poor digestion and minor urinary discomfort.

    Contains 31% Alcohol
    0.7 fl oz (20 ml)

  • PRINCIPAL DISPLAY PANEL

    62106-1107-8

    NDC 62106-1107-8

    UNDA

    numbered compounds

    UNDA 8

    Homeopathic Preparation

    For the temporary relief of symptoms
    associated with overall poor circulation.

    Contains 31% Alcohol
    0.7 fl oz (20 ml)

  • PRINCIPAL DISPLAY PANEL

    62106-1113-8

    NDC 62106-1113-8

    UNDA

    numbered compounds

    UNDA 14

    Homeopathic Preparation

    For the temporary
    relief of symptoms
    associated with
    low energy and
    common colds.

    Contains 31% Alcohol
    0.7 fl oz (20 ml)

  • PRINCIPAL DISPLAY PANEL

    62106-1158-8

    NDC 62106-1158-8

    UNDA

    numbered compounds

    UNDA 226

    Homeopathic Preparation

    For the temporary relief of symptoms associated

    with poor digestion and lack of appetite.

    Contains 31% Alcohol

    0.7 fl oz (20 ml)

  • PRINCIPAL DISPLAY PANEL

    62106-1104-8

    UNDA

    numbered compounds

    NDC 62106-1104-8

    UNDA 5

    Homeopathic Preparation

    For the temporary relief of symptoms associated with common colds.

    Contains 31% Alcohol
    0.7 fl oz (20 ml)

  • PRINCIPAL DISPLAY PANEL

    62106-1155

    NDC 62106-1155-8

    UNDA

    numbered compounds

    UNDA 212

    Homeopathic Preparation

    For the temporary relief of symptoms associated with anxiousness.

    Contains 31% Alcohol

    0.7 fl oz (20 mL)

  • INGREDIENTS AND APPEARANCE
    UNDA 8 
    hamamelis virginiana, millefolium, equisetum arvense, mercurialis perennis, thlaspi bursa-pastoris, cactus grandiflorus, crataegus, cuprum metallicum liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:62106-1107
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    HAMAMELIS VIRGINIANA BARK (UNII: IH3063S9MY) (HAMAMELIS VIRGINIANA BARK - UNII:IH3063S9MY) HAMAMELIS VIRGINIANA BARK4 [hp_X]  in 20 mL
    MERCURIALIS PERENNIS (UNII: Q35465A1MA) (MERCURIALIS PERENNIS - UNII:Q35465A1MA) MERCURIALIS PERENNIS4 [hp_X]  in 20 mL
    CRATAEGUS FRUIT (UNII: Q21UUL2105) (CRATAEGUS FRUIT - UNII:Q21UUL2105) CRATAEGUS FRUIT4 [hp_X]  in 20 mL
    COPPER (UNII: 789U1901C5) (COPPER - UNII:789U1901C5) COPPER12 [hp_X]  in 20 mL
    ACHILLEA MILLEFOLIUM (UNII: 2FXJ6SW4PK) (ACHILLEA MILLEFOLIUM - UNII:2FXJ6SW4PK) ACHILLEA MILLEFOLIUM4 [hp_X]  in 20 mL
    EQUISETUM ARVENSE BRANCH (UNII: 1L0VKZ185E) (EQUISETUM ARVENSE BRANCH - UNII:1L0VKZ185E) EQUISETUM ARVENSE BRANCH4 [hp_X]  in 20 mL
    CAPSELLA BURSA-PASTORIS (UNII: W0X9457M59) (CAPSELLA BURSA-PASTORIS - UNII:W0X9457M59) CAPSELLA BURSA-PASTORIS4 [hp_X]  in 20 mL
    SELENICEREUS GRANDIFLORUS STEM (UNII: 7114SV0MYK) (SELENICEREUS GRANDIFLORUS STEM - UNII:7114SV0MYK) SELENICEREUS GRANDIFLORUS STEM4 [hp_X]  in 20 mL
    Inactive Ingredients
    Ingredient NameStrength
    ALCOHOL (UNII: 3K9958V90M)  
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:62106-1107-81 in 1 CARTON06/02/2015
    120 mL in 1 BOTTLE, GLASS; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved homeopathic06/02/2015
    UNDA 5 
    tormentilla, tussilago farfara, adiantum capillus-veneris, glycyrrhiza glabra, drosera, grindelia, inula helenium, cuprum metallicum, argentum metallicum liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:62106-1104
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    POTENTILLA ERECTA ROOT (UNII: BI896CKT6B) (POTENTILLA ERECTA ROOT - UNII:BI896CKT6B) POTENTILLA ERECTA ROOT4 [hp_X]  in 20 mL
    ADIANTUM CAPILLUS-VENERIS LEAF (UNII: 4817H7M565) (ADIANTUM CAPILLUS-VENERIS LEAF - UNII:4817H7M565) ADIANTUM CAPILLUS-VENERIS LEAF4 [hp_X]  in 20 mL
    DROSERA ROTUNDIFOLIA FLOWERING TOP (UNII: 75O014T1HG) (DROSERA ROTUNDIFOLIA FLOWERING TOP - UNII:75O014T1HG) DROSERA ROTUNDIFOLIA FLOWERING TOP4 [hp_X]  in 20 mL
    GLYCYRRHIZA GLABRA (UNII: 2788Z9758H) (GLYCYRRHIZA GLABRA - UNII:2788Z9758H) GLYCYRRHIZA GLABRA4 [hp_X]  in 20 mL
    GRINDELIA HIRSUTULA FLOWERING TOP (UNII: IDB0NAZ6AI) (GRINDELIA HIRSUTULA FLOWERING TOP - UNII:IDB0NAZ6AI) GRINDELIA HIRSUTULA FLOWERING TOP4 [hp_X]  in 20 mL
    INULA HELENIUM ROOT (UNII: E55SMD6DA8) (INULA HELENIUM ROOT - UNII:E55SMD6DA8) INULA HELENIUM ROOT4 [hp_X]  in 20 mL
    COPPER (UNII: 789U1901C5) (COPPER - UNII:789U1901C5) COPPER12 [hp_X]  in 20 mL
    SILVER (UNII: 3M4G523W1G) (SILVER - UNII:3M4G523W1G) SILVER12 [hp_X]  in 20 mL
    TUSSILAGO FARFARA WHOLE (UNII: 6177A89GA2) (TUSSILAGO FARFARA WHOLE - UNII:6177A89GA2) TUSSILAGO FARFARA WHOLE4 [hp_X]  in 20 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    ALCOHOL (UNII: 3K9958V90M)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:62106-1104-81 in 1 CARTON06/02/2015
    120 mL in 1 BOTTLE, GLASS; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved homeopathic06/02/2015
    UNDA 14 
    eucalyptus globulus, inula helenium, jateorhiza palmata, camphora, argentum metallicum, aurum metallicum, cuprum metallicum liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:62106-1113
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    INULA HELENIUM ROOT (UNII: E55SMD6DA8) (INULA HELENIUM ROOT - UNII:E55SMD6DA8) INULA HELENIUM ROOT4 [hp_X]  in 20 mL
    JATEORHIZA CALUMBA ROOT (UNII: V36I2B8LD5) (JATEORHIZA CALUMBA ROOT - UNII:V36I2B8LD5) JATEORHIZA CALUMBA ROOT4 [hp_X]  in 20 mL
    CAMPHOR (NATURAL) (UNII: N20HL7Q941) (CAMPHOR (NATURAL) - UNII:N20HL7Q941) CAMPHOR (NATURAL)4 [hp_X]  in 20 mL
    SILVER (UNII: 3M4G523W1G) (SILVER - UNII:3M4G523W1G) SILVER12 [hp_X]  in 20 mL
    GOLD (UNII: 79Y1949PYO) (GOLD - UNII:79Y1949PYO) GOLD12 [hp_X]  in 20 mL
    COPPER (UNII: 789U1901C5) (COPPER - UNII:789U1901C5) COPPER12 [hp_X]  in 20 mL
    EUCALYPTUS GLOBULUS LEAF (UNII: S546YLW6E6) (EUCALYPTUS GLOBULUS LEAF - UNII:S546YLW6E6) EUCALYPTUS GLOBULUS LEAF4 [hp_X]  in 20 mL
    Inactive Ingredients
    Ingredient NameStrength
    ALCOHOL (UNII: 3K9958V90M)  
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:62106-1113-81 in 1 CARTON06/02/2015
    120 mL in 1 BOTTLE, GLASS; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved homeopathic06/02/2015
    UNDA 212 
    menyanthes trifoliata, viola tricolor, hydrastis canadensis, aloe socotrina liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:62106-1155
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    MENYANTHES TRIFOLIATA (UNII: 7H0QTZ446K) (MENYANTHES TRIFOLIATA - UNII:7H0QTZ446K) MENYANTHES TRIFOLIATA4 [hp_X]  in 20 mL
    VIOLA TRICOLOR (UNII: 9Q24RAI43V) (VIOLA TRICOLOR - UNII:9Q24RAI43V) VIOLA TRICOLOR4 [hp_X]  in 20 mL
    GOLDENSEAL (UNII: ZW3Z11D0JV) (GOLDENSEAL - UNII:ZW3Z11D0JV) GOLDENSEAL10 [hp_X]  in 20 mL
    ALOE (UNII: V5VD430YW9) (ALOE - UNII:V5VD430YW9) ALOE10 [hp_X]  in 20 mL
    Inactive Ingredients
    Ingredient NameStrength
    ALCOHOL (UNII: 3K9958V90M)  
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:62106-1155-81 in 1 CARTON06/02/2015
    120 mL in 1 BOTTLE, GLASS; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved homeopathic06/02/2015
    UNDA 226 
    urtica dioica, berberis vulgaris, boldo, juniperus communis, aloe socotrina, chelidonium majus liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:62106-1158
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    PEUMUS BOLDUS LEAF (UNII: Q4EWM09M3O) (PEUMUS BOLDUS LEAF - UNII:Q4EWM09M3O) PEUMUS BOLDUS LEAF6 [hp_X]  in 20 mL
    URTICA DIOICA (UNII: 710FLW4U46) (URTICA DIOICA - UNII:710FLW4U46) URTICA DIOICA6 [hp_X]  in 20 mL
    BERBERIS VULGARIS ROOT BARK (UNII: 1TH8Q20J0U) (BERBERIS VULGARIS ROOT BARK - UNII:1TH8Q20J0U) BERBERIS VULGARIS ROOT BARK6 [hp_X]  in 20 mL
    JUNIPER BERRY (UNII: O84B5194RL) (JUNIPER BERRY - UNII:O84B5194RL) JUNIPER BERRY6 [hp_X]  in 20 mL
    ALOE (UNII: V5VD430YW9) (ALOE - UNII:V5VD430YW9) ALOE6 [hp_X]  in 20 mL
    CHELIDONIUM MAJUS (UNII: 7E889U5RNN) (CHELIDONIUM MAJUS - UNII:7E889U5RNN) CHELIDONIUM MAJUS6 [hp_X]  in 20 mL
    Inactive Ingredients
    Ingredient NameStrength
    ALCOHOL (UNII: 3K9958V90M)  
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:62106-1158-81 in 1 CARTON06/02/2015
    120 mL in 1 BOTTLE, GLASS; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved homeopathic06/02/2015
    UNDA 258 
    berberis vulgaris, bryonia dioica, lycopodium clavatum, mercurialis annua, hydrastis canadensis, boldo, solidago virgaurea liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:62106-1165
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    LYCOPODIUM CLAVATUM SPORE (UNII: C88X29Y479) (LYCOPODIUM CLAVATUM SPORE - UNII:C88X29Y479) LYCOPODIUM CLAVATUM SPORE4 [hp_X]  in 20 mL
    MERCURIALIS ANNUA FLOWERING TOP (UNII: 7D28M9SL9B) (MERCURIALIS ANNUA FLOWERING TOP - UNII:7D28M9SL9B) MERCURIALIS ANNUA FLOWERING TOP4 [hp_X]  in 20 mL
    GOLDENSEAL (UNII: ZW3Z11D0JV) (GOLDENSEAL - UNII:ZW3Z11D0JV) GOLDENSEAL4 [hp_X]  in 20 mL
    PEUMUS BOLDUS LEAF (UNII: Q4EWM09M3O) (PEUMUS BOLDUS LEAF - UNII:Q4EWM09M3O) PEUMUS BOLDUS LEAF4 [hp_X]  in 20 mL
    SOLIDAGO VIRGAUREA FLOWERING TOP (UNII: 5405K23S50) (SOLIDAGO VIRGAUREA FLOWERING TOP - UNII:5405K23S50) SOLIDAGO VIRGAUREA FLOWERING TOP4 [hp_X]  in 20 mL
    BERBERIS VULGARIS ROOT BARK (UNII: 1TH8Q20J0U) (BERBERIS VULGARIS ROOT BARK - UNII:1TH8Q20J0U) BERBERIS VULGARIS ROOT BARK4 [hp_X]  in 20 mL
    BRYONIA ALBA ROOT (UNII: T7J046YI2B) (BRYONIA ALBA ROOT - UNII:T7J046YI2B) BRYONIA ALBA ROOT4 [hp_X]  in 20 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    ALCOHOL (UNII: 3K9958V90M)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:62106-1165-81 in 1 CARTON06/02/2015
    120 mL in 1 BOTTLE, GLASS; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved homeopathic06/02/2015
    Labeler - Seroyal USA (018361118)
    Establishment
    NameAddressID/FEIBusiness Operations
    SAN’UP401010287manufacture(62106-1104, 62106-1107, 62106-1113, 62106-1155, 62106-1158, 62106-1165)
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