FORMALDEHYDE - formalinum, liquid
Apotheca Company

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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Formaldehyde

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. In case of overdose, contact physician or Poison Control Center right away.

Dist. By:

Deseret Biologicals, Inc.

469 Parkland Drive

Sandy, UT 84040

www.desbio.com

PACKAGE LABEL DISPLAY:

DESBIO
NDC 57520-0802-1
HOMEOPATHIC
FORMALDEHYDE
1 FL OZ (30 ml)

Formaldehyde

FORMALDEHYDE
formalinum, liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:57520-0802
Route of Administration	ORAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
FORMALDEHYDE (UNII: 1HG84L3525) (FORMALDEHYDE - UNII:1HG84L3525)	FORMALDEHYDE	6 [hp_X] in 1 mL

Ingredient Name	Strength
Inactive Ingredients
WATER (UNII: 059QF0KO0R)
ALCOHOL (UNII: 3K9958V90M)

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:57520-0802-1	30 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
unapproved homeopathic		08/22/2011	03/30/2017

Labeler - Apotheca Company (844330915)

Registrant - Apotheca Company (844330915)

Name	Address	ID/FEI	Business Operations
Establishment
Apotheca Company		844330915	manufacture(57520-0802) , api manufacture(57520-0802) , label(57520-0802) , pack(57520-0802)

Revised: 1/2016

Document Id: ae009b3e-0ce3-4574-aa07-9c1f535c5fb4

Set id: 14d40870-2b97-450e-b8d3-1ce757423963

Version: 2

Effective Time: 20160128

Apotheca Company