ACETALDEHYDE- acetaldehyde liquid 
Deseret Biologicals, Inc.

Disclaimer: This homeopathic product has not been evaluated by the Food and Drug Administration for safety or efficacy. FDA is not aware of scientific evidence to support homeopathy as effective.

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Drug Facts:

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

ACETALDEHYDE 
acetaldehyde liquid
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:43742-0188
Route of Administration ORAL DEA Schedule     
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
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
unapproved homeopathic 11/07/2012
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)

Revised: 3/2015
Document Id: 9904a637-c24b-4d5e-8725-ef7db5f52f05
Set id: dbda1539-d0ce-4359-8e34-e4b11f8e1b8f
Version: 4
Effective Time: 20150310
 
Deseret Biologicals, Inc.