Progesterone liquid

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

Ingredients and appearance - Product information

Progesterone liquid- Progesterone

Product information

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

Active Ingredient/Active Moiety

Ingredient Name Strength
Progesterone ( UNII: 4G7DS2Q64Y)( Progesterone - UNII: 4G7DS2Q64Y ) 6 [hp_X]in 1 mL

Inactive Ingredients

Ingredient Name Code
Water ( UNII: 059QF0KO0R)
Alcohol ( UNII: 3K9958V90M)

Product Characteristics

Packaging

# Item Code Package Description Marketing Start Date
1 NDC: 43742-0158-1 30mL in 1 BOTTLE, DROPPER 2012/09/20

Marketing Information

Marketing Category Application Number or Monograph Citation Territorial Authority Marketing Start Date
unapproved homeopathic USA 2012/09/20

Labeler - Deseret Biologicals, Inc.( 940741853)

Establishment

Name ID/FEI Business Operations
Deseret Biologicals, Inc. 940741853 manufacture( 43742-0158), api manufacture( 43742-0158), label( 43742-0158), pack( 43742-0158)

Package label display:

DESBIO

NDC 43742-0158-1

HOMEOPATHIC

PROGESTERONE

1 FL OZ (30 ml)