OHM MENOPAUSE- ammonium carbonicum, amyl nitrosum, cimicifuga racemosa, glonoinum, lachesis mutus, sanguinaria, canadensis. liquid

OHM Menopause by

Drug Labeling and Warnings

OHM Menopause by is a Homeopathic medication manufactured, distributed, or labeled by OHM PHARMA INC.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

ACTIVE INGREDIENTS (HPUS*): Equal amounts of: Ammonium Carbonicum 12C, Amyl Nitrosum 6X, Cimicifuga Racemosa 3X, Glonoinum 12X, Lachesis Mutus 12X, Sanguinaria Canadensis 4X.

*The letters "HPUS" indicate that the components in this product are officially monographed in the Homeopathic Pharmacopeia of the United States.

INDICATIONS & USAGE

USES: Temporarily relieves symptoms caused by common menopause, hormonal imbalances.

**​This statement has not been evaluated by the FDA. It is based on documented Homeopathic Materia Medica.

WARNINGS

WARNINGS: IF PREGNANT OR BREAST-FEEDING, ask a health professional before use. If symptoms worsen or persist for more than a week, discontinue use and contact a doctor

• ​KEEP OUT OF REACH OF CHILDREN.

DOSAGE & ADMINISTRATION

DIRECTIONS: Shake 10 times before use. Hold close to mouth and spray 3 times directly under the tongue 2-3 times a day, or as directed by a health care professional. Not for use by children.

OTHER SAFETY INFORMATION

Do not use if cap seal is broken.

INACTIVE INGREDIENT

INACTIVE INGREDIENTS: Organic Alcohol 15% (Non-GMO, Kosher Certified, Corn, Gluten, Allergen Free), Purified Water, Vegetable Glycerin 15%.

QUESTIONS

Mfg. By: OHM PHARMA, INC. Mineral Wells, TX 76067

www.ohmpharma.com

PRINCIPAL DISPLAY PANEL

HOMEOPATHIC MEDICINE

NDC: 66096-156-05

MENOPAUSE

Natural - Safe - Effective

No Side Effects

2 fl oz (59mL) / 15% Alcohol

PRODUCT OF USA

Temporarily relieves symptoms caused by common menopause.

INGREDIENTS AND APPEARANCE

OHM MENOPAUSE 
ammonium carbonicum, amyl nitrosum, cimicifuga racemosa, glonoinum, lachesis mutus, sanguinaria, canadensis. liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 66096-156
Route of Administration	ORAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
AMMONIUM CARBONATE (UNII: NJ5VT0FKLJ) (AMMONIUM CATION - UNII:54S68520I4)	AMMONIUM CARBONATE	12 [hp_C]  in 59 mL
AMYL NITRITE (UNII: 22T8Z09XAK) (AMYL NITRITE - UNII:22T8Z09XAK)	AMYL NITRITE	6 [hp_X]  in 59 mL
BLACK COHOSH (UNII: K73E24S6X9) (BLACK COHOSH - UNII:K73E24S6X9)	BLACK COHOSH	3 [hp_X]  in 59 mL
NITROGLYCERIN (UNII: G59M7S0WS3) (NITROGLYCERIN - UNII:G59M7S0WS3)	NITROGLYCERIN	12 [hp_X]  in 59 mL
LACHESIS MUTA VENOM (UNII: VSW71SS07I) (LACHESIS MUTA VENOM - UNII:VSW71SS07I)	LACHESIS MUTA VENOM	12 [hp_X]  in 59 mL
SANGUINARIA CANADENSIS ROOT (UNII: N9288CD508) (SANGUINARIA CANADENSIS ROOT - UNII:N9288CD508)	SANGUINARIA CANADENSIS ROOT	4 [hp_X]  in 59 mL

Inactive Ingredients
Ingredient Name	Strength
ALCOHOL (UNII: 3K9958V90M)
WATER (UNII: 059QF0KO0R)
GLYCERIN (UNII: PDC6A3C0OX)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 66096-156-05	59 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	08/19/2015

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved homeopathic		08/19/2015

Labeler - OHM PHARMA INC. (030572478)

Registrant - OHM PHARMA INC. (030572478)

Establishment
Name	Address	ID/FEI	Business Operations
OHM PHARMA INC.		030572478	manufacture(66096-156)