Eczema Relief: Homeopathic Product Information

ECZEMA RELIEF- arsenic triiodide, potassium bromide, potassium chloride, sodium bromide, nickel sulfate hexahydrate, sulfur iodide, viola tricolor and zinc bromide 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.

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
(click image for full-size original)

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 Type HUMAN OTC DRUG Item Code (Source) NDC:66096-192
Route of Administration ORAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
ARSENIC TRIIODIDE (ARSENIC CATION (3+)) ARSENIC TRIIODIDE 8 [hp_X] in 59 mL
POTASSIUM BROMIDE (BROMIDE ION) POTASSIUM BROMIDE 4 [hp_X] in 59 mL
POTASSIUM CHLORIDE (POTASSIUM CATION) POTASSIUM CHLORIDE 4 [hp_X] in 59 mL
SODIUM BROMIDE (BROMIDE ION) SODIUM BROMIDE 4 [hp_X] in 59 mL
NICKEL SULFATE HEXAHYDRATE (NICKEL CATION) NICKEL SULFATE HEXAHYDRATE 5 [hp_X] in 59 mL
SULFUR IODIDE (SULFUR IODIDE) SULFUR IODIDE 14 [hp_X] in 59 mL
VIOLA TRICOLOR (VIOLA TRICOLOR) VIOLA TRICOLOR 12 [hp_X] in 59 mL
ZINC BROMIDE (ZINC CATION) ZINC BROMIDE 6 [hp_X] in 59 mL
Inactive Ingredients
Ingredient Name Strength
ALCOHOL
WATER
GLYCERIN
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:66096-192-05 59 mL in 1 PACKAGE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
unapproved homeopathic 05/22/2015
Labeler — OHM PHARMA INC. (030572478)

Revised: 12/2021 OHM PHARMA INC.

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