COUGH RELIEF- aconitum nap, antimon crud, antimon sulph, antimon tart, aralia rac, bryonia, chelidonium maj, cuprum met, drosera, hepar sulph calc, kali carb, spongia. liquid

Cough Relief by

Drug Labeling and Warnings

Cough Relief 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: Aconitum Nap 6X, Antimon Crud 8X, Antimon Sulph 16X, Antimon Tart 8X, Aralia Rac 4X, Bryonia 6X, Chelidonium Maj 6X, Cuprum Met 12X, Drosera 6X, Hepar Sulph Calc 12X, Kali Carb 12X, Spongia 6X.

*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 cough symptoms of diverse origins.

**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. Adults & children above 12 years of age: spray 3-4 times under the tongue every 15 minutes, extend intervals as symptoms improve or as directed by a health care professional. Children under 12: use half the adult dose.

OTHER SAFETY INFORMATION

Do not use if cap seal is broken.

INACTIVE INGREDIENT

INACTIVE INGREDIENTS: Ethanol 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: 66096-115-05

COUGH Relief

Natural - Safe - Effective

No Side Effects

2 fl oz (59mL) / 15% Alcohol

PRODUCT OF USA

Temporarily relieves cough.

INGREDIENTS AND APPEARANCE

COUGH RELIEF 
aconitum nap, antimon crud, antimon sulph, antimon tart, aralia rac, bryonia, chelidonium maj, cuprum met, drosera, hepar sulph calc, kali carb, spongia. liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 66096-115
Route of Administration	ORAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ACONITUM NAPELLUS (UNII: U0NQ8555JD) (ACONITUM NAPELLUS - UNII:U0NQ8555JD)	ACONITUM NAPELLUS	6 [hp_X]  in 59 mL
ANTIMONY TRISULFIDE (UNII: F79059A38U) (ANTIMONY TRISULFIDE - UNII:F79059A38U)	ANTIMONY TRISULFIDE	8 [hp_X]  in 59 mL
ANTIMONY PENTASULFIDE (UNII: 1433F1I86N) (ANTIMONY PENTASULFIDE - UNII:1433F1I86N)	ANTIMONY PENTASULFIDE	8 [hp_X]  in 59 mL
ANTIMONY POTASSIUM TARTRATE (UNII: DL6OZ476V3) (ANTIMONY CATION (3+) - UNII:069647RPT5)	ANTIMONY POTASSIUM TARTRATE	8 [hp_X]  in 59 mL
ARALIA RACEMOSA ROOT (UNII: T90W4582DU) (ARALIA RACEMOSA ROOT - UNII:T90W4582DU)	ARALIA RACEMOSA ROOT	4 [hp_X]  in 59 mL
BRYONIA ALBA ROOT (UNII: T7J046YI2B) (BRYONIA ALBA ROOT - UNII:T7J046YI2B)	BRYONIA ALBA ROOT	6 [hp_X]  in 59 mL
CHELIDONIUM MAJUS (UNII: 7E889U5RNN) (CHELIDONIUM MAJUS - UNII:7E889U5RNN)	CHELIDONIUM MAJUS	6 [hp_X]  in 59 mL
COPPER (UNII: 789U1901C5) (COPPER - UNII:789U1901C5)	COPPER	12 [hp_X]  in 59 mL
DROSERA ROTUNDIFOLIA (UNII: QR44N9XPJQ) (DROSERA ROTUNDIFOLIA - UNII:QR44N9XPJQ)	DROSERA ROTUNDIFOLIA	6 [hp_X]  in 59 mL
CALCIUM SULFIDE (UNII: 1MBW07J51Q) (CALCIUM SULFIDE - UNII:1MBW07J51Q)	CALCIUM SULFIDE	12 [hp_X]  in 59 mL
POTASSIUM CARBONATE (UNII: BQN1B9B9HA) (CARBONATE ION - UNII:7UJQ5OPE7D)	POTASSIUM CARBONATE	12 [hp_X]  in 59 mL
SPONGIA OFFICINALIS SKELETON, ROASTED (UNII: 1PIP394IID) (SPONGIA OFFICINALIS SKELETON, ROASTED - UNII:1PIP394IID)	SPONGIA OFFICINALIS SKELETON, ROASTED	6 [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: 66096-115-05	59 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	05/21/2015

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved homeopathic		05/21/2015

Labeler - OHM PHARMA INC. (030572478)

Registrant - OHM PHARMA INC. (030572478)

Establishment
Name	Address	ID/FEI	Business Operations
OHM PHARMA INC.		030572478	manufacture(66096-115)