PROGESTERONE- progesterone 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.

----------

DRUG FACTS:

ACTIVE INGREDIENTS:

Progesterone 6X, 12X, 30X, 200X, 12C, 30C, 60C, 200C.

PURPOSE:

Progesterone - Mood Swings, Painful Menses, Nervousness, Hot Flashes, Headache, Breast Tenderness, Breast Pain, Back Pain, Leg Pain

USES:

• For the temporary relief of symptoms including:

• mood swings • painful menses • nervousness 

• hot flashes • headache • breast tenderness

• breast pain • back pain • let pain

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

WARNINGS:

If pregnant or breast-feeding, seek advice of a health professional before use.

Keep out of reach of children. In case of overdose, contact a physician or Poison Control Center right away.

Tamper Evident: Sealed for your protection. Do not use if seal is broken or missing.

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, 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

QUESTIONS:

Dist. By: Deseret Biologicals, Inc.

469 W. Parkland Drive

Sandy, UT 84070

www.desbio.com

800-827-8204

PACKAGE LABEL DISPLAY:

DesBio

Progesterone

Homeopathic

NDC 43742-0851-1

1 FL OZ (30 ml)

Progesterone

PROGESTERONE 
progesterone liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:43742-0851
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
PROGESTERONE (UNII: 4G7DS2Q64Y) (PROGESTERONE - UNII:4G7DS2Q64Y) PROGESTERONE6 [hp_X]  in 1 mL
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
ALCOHOL (UNII: 3K9958V90M)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:43742-0851-130 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product09/19/2016
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
unapproved homeopathic09/19/2016
Labeler - Deseret Biologicals, Inc. (940741853)
Registrant - Apotheca Company (844330915)
Establishment
NameAddressID/FEIBusiness Operations
Apotheca Company844330915manufacture(43742-0851) , api manufacture(43742-0851) , label(43742-0851) , pack(43742-0851)

Revised: 3/2024
Document Id: f85df087-4485-48ab-887c-9705ddabd166
Set id: ef33af80-5f72-4635-a8ae-f48376efb451
Version: 2
Effective Time: 20240314
 
Deseret Biologicals, Inc.