CAFFEIC ACID LIQUID [DESERET BIOLOGICALS, INC.]

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  • CAFFEIC ACID LIQUID [DESERET BIOLOGICALS, INC.]

CAFFEIC ACID LIQUID [DESERET BIOLOGICALS, INC.]
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NDC 43742-0219-1
Set ID d485d6b0-2600-43f6-87f9-09f89c9a717c
Category HUMAN OTC DRUG LABEL
Packager Deseret Biologicals, Inc.
Generic Name
Product Class
Product Number
Application Number
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  • ACTIVE INGREDIENTS

    Caffeic Acid 6X, 12X, 30X, 200X, 12C, 30C, 60C, 200C

  • INDICATIONS

    For temporary relief of sinus congestion, headache, indigestion, joint pains, dizziness, tingling nd numbness of extremities. 

  • WARNINGS

    Keep out of reach of children.  In case of overdose, contact physician or Poison Control Center right away. 

    If pregnant or breast-feeding, seek advice of a health professional before use. 

    Tamper seal:  Sealed for Your Protection.  Do not use if seal is broken or missing. 

  • DIRECTIONS

    1-10 drops under the tongue, 3 times a day or as directed by a health professional. Consult a physician for use in children under 12 years of age.

  • INACTIVE INGREDIENTS

    Demineralized water, 25% Ethanol.

  • KEEP OUT OF REACH OF CHILDREN

    Keep out of reach of children. In case of overdose, contact physician or Poison Control Center right away.

  • INDICATIONS AND USAGE

    For temporary relief of sinus congestion, headache, indigestion, joint pains, dizziness, tingling nd numbness of extremities.

  • QUESTIONS

    Dist. By: Deseret Biologicals, Inc.

    469 Parkland Drive

    Sandy, UT 84070

    www.desbio.com

  • PACKAGE LABEL DISPLAY:

    DESBIO

    NDC 43742-0219-1

    HOMEOPATHIC

    CAFFEIC ACID

    1 FL OZ (30 ml)

    Caffeic Acid

  • INGREDIENTS AND APPEARANCE
    CAFFEIC ACID 
    caffeic acid liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:43742-0219
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    CAFFEIC ACID (UNII: U2S3A33KVM) (CAFFEIC ACID - UNII:U2S3A33KVM) CAFFEIC ACID6 [hp_X]  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    ALCOHOL (UNII: 3K9958V90M)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:43742-0219-130 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product04/08/2013
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved homeopathic04/08/201305/27/2020
    Labeler - Deseret Biologicals, Inc. (940741853)
    Registrant - Apotheca Company (844330915)
    Establishment
    NameAddressID/FEIBusiness Operations
    Apotheca Company844330915manufacture(43742-0219) , api manufacture(43742-0219) , label(43742-0219) , pack(43742-0219)
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