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Acetaldehyde (Deseret Biologicals, Inc.)

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LIQUID 30 mL in 1 BOTTLE, DROPPER (43742-0188-1) Label Information

Complete Acetaldehyde Information

  • ACTIVE INGREDIENTS:

    Acetaldehyde 6X, 12X, 30X, 200X, 12C, 30C, 60C, 200C.


  • INDICATIONS:

    For temporary relief of symptoms caused by allergic reaction from perfumes, flavors, dyes, plastics, alcohol or foods including sneezing, headache, bronchitis, difficult breathing and digestive malfunction.


  • WARNINGS:

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


  • INDICATIONS:

    For temporary relief of symptoms caused by allergic reaction from perfumes, flavors, dyes, plastics, alcohol or foods including sneezing, headache, bronchitis, difficult breathing and digestive malfunction.


  • QUESTIONS:

    Dist. By: Deseret Biologicals, Inc.

    469 W. Parkland Drive

    Sandy, UT 84070

    www.desbio.com


  • PACKAGE LABEL DISPLAY:

    DESBIO

    NDC 43742-0188-1

    HOMEOPATHIC

    ACETALDEHYDE

    1 FL OZ (30 ml)

    Acetaldehyde


  • INGREDIENTS AND APPEARANCE
    ACETALDEHYDE 
    acetaldehyde liquid
    Product Information
    Product Type HUMAN OTC DRUG Item Code (Source) NDC:43742-0188
    Route of Administration ORAL
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    ACETALDEHYDE (UNII: GO1N1ZPR3B) (ACETALDEHYDE - UNII:GO1N1ZPR3B) ACETALDEHYDE 6 [hp_X]  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    WATER (UNII: 059QF0KO0R)  
    ALCOHOL (UNII: 3K9958V90M)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:43742-0188-1 30 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product 11/07/2012
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    unapproved homeopathic 11/07/2012 12/08/2020
    Labeler - Deseret Biologicals, Inc. (940741853)
    Registrant - Apotheca Company (844330915)
    Establishment
    Name Address ID/FEI Business Operations
    Apotheca Company 844330915 manufacture(43742-0188) , api manufacture(43742-0188) , pack(43742-0188) , label(43742-0188)