Progesterone by Deseret Biologicals, Inc. / Apotheca Company PROGESTERONE liquid

Progesterone by

Drug Labeling and Warnings

Progesterone by is a Homeopathic medication manufactured, distributed, or labeled by Deseret Biologicals, Inc., Apotheca Company. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENTS

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

INDICATIONS

For temporary relief of allergic reaction to dairy and milk products, mood swings, painful menses, nervousness, hot flashes, headache, breast tenderness and pain, back and leg 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

KEEP OUT OF REACH OF CHILDREN:  In case of overdose, contact physician or Poison Control Center right away.

INDICATIONS AND USAGE

For temporary relief of allergic reaction to dairy and milk products, mood swings, painful menses, nervousness, hot flashes, headache, breast tenderness and pain, back and leg pain.**

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

QUESTIONS

Dist. By: Deseret Biologicals, Inc.

469 Parkland Drive

Sandy, UT 84070

www.desbio.com

PACKAGE LABEL DISPLAY:

DESBIO

NDC: 43742-0158-1

HOMEOPATHIC

PROGESTERONE

1 FL OZ (30 ml)

INGREDIENTS AND APPEARANCE

PROGESTERONE 
progesterone liquid

Product Information
Product Type	HUMAN PRESCRIPTION DRUG	Item Code (Source)	NDC: 43742-0158
Route of Administration	ORAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
PROGESTERONE (UNII: 4G7DS2Q64Y) (PROGESTERONE - UNII:4G7DS2Q64Y)	PROGESTERONE	6 [hp_X]  in 1 mL

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

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 43742-0158-1	30 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product	09/20/2012

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved homeopathic		09/20/2012	12/22/2020

Labeler - Deseret Biologicals, Inc. (940741853)

Registrant - Apotheca Company (844330915)

Establishment
Name	Address	ID/FEI	Business Operations
Apotheca Company		844330915	manufacture(43742-0158) , api manufacture(43742-0158) , label(43742-0158) , pack(43742-0158)