NDC | 62750-001-11, 62750-001-12 |
Set ID | 04d551dc-23f9-414b-aac4-e92d111c867d |
Category | HUMAN OTC DRUG LABEL |
Packager | Matrixx Initiatives, Inc. |
Generic Name | |
Product Class | |
Product Number | |
Application Number |
- SPL UNCLASSIFIED SECTION
- Active ingredients
- Purpose
- Uses
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Warnings
For nasal use only.
Ask a doctor before use if you have
- ear, nose, or throat sensitivity
- susceptibility to nosebleeds
- breathing problems such as emphysema or chronic bronchitis
When using this product
- avoid contact with eyes. Rinse right away with water if it gets in eyes and seek medical help right away.
- the use of this container by more than one person may spread infection
- temporary discomfort such as burning, stinging, sneezing, or an increase in nasal discharge may occur
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Directions
- adults and children 12 years of age and older:
- remove cap and safety clip (also see illustrations on side of carton)
- hold with thumb at bottom of bottle and nozzle between your fingers
- before using the first time, prime pump by depressing several times
- place tip of nozzle just past nasal opening (approximately 1/8")
- while inside nasal opening, slightly angle nozzle outward
- pump once into each nostril
- after application, press lightly on outside of each nostril for about 5 seconds
- wait at least 30 seconds before blowing nose
- use once every 4 hours
- optimal results may not be seen for 1-2 weeks. After 1-2 weeks, you may need to use only 1-2 times daily. For best results, use up to 1 week before contact with known causes of your allergies.
- children under 12 years of age: ask a doctor
- adults and children 12 years of age and older:
- Other information
- Inactive ingredients
- Questions? Comments? Side Effects?
- SPL UNCLASSIFIED SECTION
- PRINCIPAL DISPLAY PANEL - 15 mL Bottle Carton
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INGREDIENTS AND APPEARANCE
ZICAM ALLERGY RELIEF
galphimia glauca flowering top, histamine dihydrochloride, luffa operculata fruit, and sulfur sprayProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:62750-001 Route of Administration NASAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength galphimia glauca flowering top (UNII: 93PH5Q8M7E) (galphimia glauca flowering top - UNII:93PH5Q8M7E) galphimia glauca flowering top 30 [hp_X] in 1 mL histamine dihydrochloride (UNII: 3POA0Q644U) (histamine - UNII:820484N8I3) histamine dihydrochloride 200 [hp_X] in 1 mL luffa operculata fruit (UNII: C4MO6809HU) (luffa operculata fruit - UNII:C4MO6809HU) luffa operculata fruit 30 [hp_X] in 1 mL sulfur (UNII: 70FD1KFU70) (sulfur - UNII:70FD1KFU70) sulfur 200 [hp_X] in 1 mL Inactive Ingredients Ingredient Name Strength benzalkonium chloride (UNII: F5UM2KM3W7) benzyl alcohol (UNII: LKG8494WBH) edetate disodium (UNII: 7FLD91C86K) glycerin (UNII: PDC6A3C0OX) HYDROXYETHYL CELLULOSE (100 MPA.S AT 2%) (UNII: R33S7TK2EP) potassium chloride (UNII: 660YQ98I10) potassium phosphate, unspecified form (UNII: B7862WZ632) water (UNII: 059QF0KO0R) sodium chloride (UNII: 451W47IQ8X) sodium phosphate (UNII: SE337SVY37) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:62750-001-11 1 in 1 CARTON 04/14/2000 1 15 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 2 NDC:62750-001-12 1 in 1 CARTON 04/14/2000 2 30 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date UNAPPROVED HOMEOPATHIC 04/14/2000 Labeler - Matrixx Initiatives, Inc. (790037253) Establishment Name Address ID/FEI Business Operations Accupac, Inc. 071609663 MANUFACTURE(62750-001)