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 
OHM PHARMA 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.

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OHM Cough Relief

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.

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: 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.

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.

Do not use if cap seal is broken.

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

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

www.ohmpharma.com

HOMEOPATHIC MEDICINE

NDC: 66096-115-05

COUGH Relief

Natural - Safe - Effective

No Side Effects

2 fl oz (59mL) / 15% Alcohol

PRODUCT OF USA

2oz bottle label

Temporarily relieves cough.

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 TypeHUMAN OTC DRUGItem Code (Source)NDC:66096-115
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ACONITUM NAPELLUS (UNII: U0NQ8555JD) (ACONITUM NAPELLUS - UNII:U0NQ8555JD) ACONITUM NAPELLUS6 [hp_X]  in 59 mL
ANTIMONY TRISULFIDE (UNII: F79059A38U) (ANTIMONY TRISULFIDE - UNII:F79059A38U) ANTIMONY TRISULFIDE8 [hp_X]  in 59 mL
ANTIMONY PENTASULFIDE (UNII: 1433F1I86N) (ANTIMONY PENTASULFIDE - UNII:1433F1I86N) ANTIMONY PENTASULFIDE8 [hp_X]  in 59 mL
ANTIMONY POTASSIUM TARTRATE (UNII: DL6OZ476V3) (ANTIMONY CATION (3+) - UNII:069647RPT5) ANTIMONY POTASSIUM TARTRATE8 [hp_X]  in 59 mL
ARALIA RACEMOSA ROOT (UNII: T90W4582DU) (ARALIA RACEMOSA ROOT - UNII:T90W4582DU) ARALIA RACEMOSA ROOT4 [hp_X]  in 59 mL
BRYONIA ALBA ROOT (UNII: T7J046YI2B) (BRYONIA ALBA ROOT - UNII:T7J046YI2B) BRYONIA ALBA ROOT6 [hp_X]  in 59 mL
CHELIDONIUM MAJUS (UNII: 7E889U5RNN) (CHELIDONIUM MAJUS - UNII:7E889U5RNN) CHELIDONIUM MAJUS6 [hp_X]  in 59 mL
COPPER (UNII: 789U1901C5) (COPPER - UNII:789U1901C5) COPPER12 [hp_X]  in 59 mL
DROSERA ROTUNDIFOLIA (UNII: QR44N9XPJQ) (DROSERA ROTUNDIFOLIA - UNII:QR44N9XPJQ) DROSERA ROTUNDIFOLIA6 [hp_X]  in 59 mL
CALCIUM SULFIDE (UNII: 1MBW07J51Q) (CALCIUM SULFIDE - UNII:1MBW07J51Q) CALCIUM SULFIDE12 [hp_X]  in 59 mL
POTASSIUM CARBONATE (UNII: BQN1B9B9HA) (CARBONATE ION - UNII:7UJQ5OPE7D) POTASSIUM CARBONATE12 [hp_X]  in 59 mL
SPONGIA OFFICINALIS SKELETON, ROASTED (UNII: 1PIP394IID) (SPONGIA OFFICINALIS SKELETON, ROASTED - UNII:1PIP394IID) SPONGIA OFFICINALIS SKELETON, ROASTED6 [hp_X]  in 59 mL
Inactive Ingredients
Ingredient NameStrength
ALCOHOL (UNII: 3K9958V90M)  
WATER (UNII: 059QF0KO0R)  
GLYCERIN (UNII: PDC6A3C0OX)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:66096-115-0559 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product05/21/2015
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
unapproved homeopathic05/21/2015
Labeler - OHM PHARMA INC. (030572478)

Revised: 12/2021
Document Id: d44af2b7-f773-3d27-e053-2a95a90abc46
Set id: 991fd747-7a46-4689-afac-381c57b91e05
Version: 4
Effective Time: 20211229
 
OHM PHARMA INC.