ECZEMA RELIEF- arsenicum iodatum, kali bromatum, kali muriaticum, natrum bromatum, niccolum sulphuricum, sulphur iodatum, viola tricolor, zincum bromatum. 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 Eczema Relief

ACTIVE INGREDIENTS (HPUS*): Equal amounts of : Arsenicum Iodatum 8X, Kali Bromatum 4X, Kali Muriaticum 4X, Natrum Bromatum 4X, Niccolum Sulphuricum 5X, Sulphur Iodatum 14X, Viola Tricolor 12X, Zincum Bromatum 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 eczema - psoriatic skin symptoms.**

​**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 care 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 2-3 times a day, 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: 66096-192-05

ECZEMA Relief

Natural - Safe - Effective

No Side Effects

2 fl oz (59 mL) / 15% Alcohol

PRODUCT OF USA

2oz bottle label

Temporarily relieves eczema.

ECZEMA RELIEF 
arsenicum iodatum, kali bromatum, kali muriaticum, natrum bromatum, niccolum sulphuricum, sulphur iodatum, viola tricolor, zincum bromatum. liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:66096-192
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ARSENIC TRIIODIDE (UNII: 3029988O2T) (ARSENIC CATION (3+) - UNII:C96613F5AV) ARSENIC TRIIODIDE8 [hp_X]  in 59 mL
POTASSIUM BROMIDE (UNII: OSD78555ZM) (BROMIDE ION - UNII:952902IX06) POTASSIUM BROMIDE4 [hp_X]  in 59 mL
POTASSIUM CHLORIDE (UNII: 660YQ98I10) (POTASSIUM CATION - UNII:295O53K152) POTASSIUM CHLORIDE4 [hp_X]  in 59 mL
SODIUM BROMIDE (UNII: LC1V549NOM) (BROMIDE ION - UNII:952902IX06) SODIUM BROMIDE4 [hp_X]  in 59 mL
NICKEL SULFATE HEXAHYDRATE (UNII: JC9WZ4FK68) (NICKEL CATION - UNII:OIS2CXW7AM) NICKEL SULFATE HEXAHYDRATE5 [hp_X]  in 59 mL
SULFUR IODIDE (UNII: L6L8KA2AA0) (SULFUR IODIDE - UNII:L6L8KA2AA0) SULFUR IODIDE14 [hp_X]  in 59 mL
VIOLA TRICOLOR (UNII: 9Q24RAI43V) (VIOLA TRICOLOR - UNII:9Q24RAI43V) VIOLA TRICOLOR12 [hp_X]  in 59 mL
ZINC BROMIDE (UNII: OO7ZBU9703) (ZINC CATION - UNII:13S1S8SF37) ZINC BROMIDE6 [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:66096-192-0559 mL in 1 PACKAGE; Type 0: Not a Combination Product05/22/2015
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
unapproved homeopathic05/22/2015
Labeler - OHM PHARMA INC. (030572478)

Revised: 12/2021
Document Id: d44acb83-411f-5445-e053-2995a90a6760
Set id: 92077b39-ed44-4d73-865f-0ec83e994940
Version: 4
Effective Time: 20211229
 
OHM PHARMA INC.