TESTOSTERONE- testosterone, 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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Testosterone

ACTIVE INGREDIENTS: Testosterone 6X, 12X, 30X, 200X, 12C, 30C, 60C, 200C.

INDICATIONS: For temporary relief of symptoms related to testosterone sensitivity including gastritis, weak libido, prostatitis, stress, memory loss, infertility, stomach discomfort, impotence and general joint pain.**

**These statements are based upon homeopathic principles. They have not been reviewed by the Food and Drug Administration.

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.

**These statements are based upon homeopathic principles. They have not been reviewed by the Food and Drug Administration.

Dist. By:

Deseret Biologicals, Inc.

469 Parkland Drive

Sandy, UT 84070

www.desbio.com

DESBIO

NDC 43742-0021-1

HOMEOPATHIC

TESTOSTERONE

1 FL OZ (30 ml)

Testosterone

TESTOSTERONE
testosterone, liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:43742-0021
Route of Administration	ORAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
TESTOSTERONE (UNII: 3XMK78S47O) (TESTOSTERONE - UNII:3XMK78S47O)	TESTOSTERONE	6 [hp_X] in 1 mL

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

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:43742-0021-1	30 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product	04/26/2012	10/27/2020

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
unapproved homeopathic		04/26/2012	10/27/2020

Labeler - Deseret Biologicals, Inc. (940741853)

Registrant - Apotheca Company (844330915)

Name	Address	ID/FEI	Business Operations
Establishment
Apotheca Company		844330915	manufacture(43742-0021) , api manufacture(43742-0021) , label(43742-0021) , pack(43742-0021)

Revised: 9/2018

Document Id: 004bf611-884b-46f3-88cb-f7b515dd2e2b

Set id: 748747b6-03a9-4aa0-9493-bf9731f89d8b

Version: 3

Effective Time: 20180914

Deseret Biologicals, Inc.