DHEA- dhea (dehydroepiandrosterone) 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 INGREDIENT:

DHEA (DEHYDROEPIANDROSTERONE) 6X, 12X, 30X, 200X, 12C, 30C, 60C, 200C

HOMEOPATHIC INDICATIONS:

For temporary relief of symptoms related to adrenal glands such as fatigue and low energy.**

**These statements are based upon traditional 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 a physician or Poison Control Center right away.

If pregnant or breast-feeding, ask a health professional before use.

Tamper seal: "Sealed for Your Protection."

Do not use if seal is broken or missing.

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.

DIRECTIONS:

1-10 drops under the tongue, 2 times a day or as directed by a health professional. Consult a physician for use in children under 12 years of age.

HOMEOPATHIC INDICATIONS:

For temporary relief of symptoms related to adrenal glands such as fatigue and low energy.**

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

INACTIVE INGREDIENTS:

Demineralized Water, 25% Ethanol

QUESTIONS:

Dist. By: Deseret Biologicals, Inc.

469 W. Parkland Drive

Sandy, UT 84070 www.desbio.com

PACKAGE LABEL DISPLAY:

DESBIO


NDC 43742-0564-1
HOMEOPATHIC


DHEA


1 FL OZ (30 ml)

DHEA

DHEA 
dhea (dehydroepiandrosterone) liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:43742-0564
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
PRASTERONE (UNII: 459AG36T1B) (PRASTERONE - UNII:459AG36T1B) PRASTERONE6 [hp_X]  in 1 mL
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
ALCOHOL (UNII: 3K9958V90M)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:43742-0564-130 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product01/19/2015
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
unapproved homeopathic01/19/2015
Labeler - Deseret Biologicals, Inc. (940741853)
Registrant - Apotheca Company (844330915)
Establishment
NameAddressID/FEIBusiness Operations
Apotheca Company844330915manufacture(43742-0564) , api manufacture(43742-0564) , label(43742-0564) , pack(43742-0564)

Revised: 1/2024
Document Id: 4d37b241-11ac-4d8a-8e2c-64aa1b65cad1
Set id: d6edd874-495c-4eb5-bf3d-72c2ee41fc88
Version: 5
Effective Time: 20240115
 
Deseret Biologicals, Inc.