FORMALDEHYDE- formalinum 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:

Formalinum 6X, 12X, 30X, 200X, 12C, 30C, 60C, 200C

INDICATIONS:

For temporary relief of reactions related to formaldehyde sensitivity including asthma, burning eyes, crying, depression, dizziness, muscle spasms, rapid heart beat, shakiness and throat inflammation.

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:

For temporary relief of reactions related to formaldehyde sensitivity including asthma, burning eyes, crying, depression, dizziness, muscle spasms, rapid heart beat, shakiness and throat inflammation.

QUESTIONS:

Dist. By: Deseret Biologicals, Inc.

469 W. Parkland Drive

Sandy, UT 84070

www.desbio.com

PACKAGE LABEL DISPLAY:

DESBIO

NDC 43742-0105-1

HOMEOPATHIC

FORMALDEHYDE

1 FL OZ (30 ml)

FORMALDEHYDE

FORMALDEHYDE 
formalinum liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:43742-0105
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
FORMALDEHYDE (UNII: 1HG84L3525) (FORMALDEHYDE - UNII:1HG84L3525) FORMALDEHYDE6 [hp_X]  in 1 mL
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
ALCOHOL (UNII: 3K9958V90M)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:43742-0105-130 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product12/28/2012
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
unapproved homeopathic12/28/201207/29/2020
Labeler - Deseret Biologicals, Inc. (940741853)
Registrant - Apotheca Company (844330915)
Establishment
NameAddressID/FEIBusiness Operations
Apotheca Company844330915manufacture(43742-0105) , api manufacture(43742-0105) , label(43742-0105) , pack(43742-0105)

Revised: 6/2016
 
Deseret Biologicals, Inc.