Eczema Relief (Arsenicum Iodatum, Kali Bromatum, Kali Muriaticum, Natrum Bromatum, Niccolum Sulphuricum, Sulphur Iodatum, Viola Tricolor, Zincum Bromatum.) Liquid [Ohm Pharma Inc.] -

ECZEMA RELIEF (ARSENICUM IODATUM, KALI BROMATUM, KALI MURIATICUM, NATRUM BROMATUM, NICCOLUM SULPHURICUM, SULPHUR IODATUM, VIOLA TRICOLOR, ZINCUM BROMATUM.) LIQUID [OHM PHARMA INC.]
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NDC	66096-192-05
Set ID	92077b39-ed44-4d73-865f-0ec83e994940
Category	HUMAN OTC DRUG LABEL
Packager	OHM PHARMA INC.
Generic Name
Product Class
Product Number
Application Number

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ACTIVE INGREDIENT

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.
INDICATIONS & USAGE

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
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.
DOSAGE & ADMINISTRATION

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.
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: 66096-192-05

ECZEMA Relief

Natural - Safe - Effective

No Side Effects

2 fl oz (59 mL) / 15% Alcohol

PRODUCT OF USA

Temporarily relieves eczema.

INGREDIENTS AND APPEARANCE

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

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
ARSENIC TRIIODIDE (UNII: 3029988O2T) (ARSENIC CATION (3+) - UNII:C96613F5AV)	ARSENIC TRIIODIDE	8 [hp_X] in 59 mL
POTASSIUM BROMIDE (UNII: OSD78555ZM) (BROMIDE ION - UNII:952902IX06)	POTASSIUM BROMIDE	4 [hp_X] in 59 mL
POTASSIUM CHLORIDE (UNII: 660YQ98I10) (POTASSIUM CATION - UNII:295O53K152)	POTASSIUM CHLORIDE	4 [hp_X] in 59 mL
SODIUM BROMIDE (UNII: LC1V549NOM) (BROMIDE ION - UNII:952902IX06)	SODIUM BROMIDE	4 [hp_X] in 59 mL
NICKEL SULFATE HEXAHYDRATE (UNII: JC9WZ4FK68) (NICKEL CATION - UNII:OIS2CXW7AM)	NICKEL SULFATE HEXAHYDRATE	5 [hp_X] in 59 mL
SULFUR IODIDE (UNII: L6L8KA2AA0) (SULFUR IODIDE - UNII:L6L8KA2AA0)	SULFUR IODIDE	14 [hp_X] in 59 mL
VIOLA TRICOLOR (UNII: 9Q24RAI43V) (VIOLA TRICOLOR - UNII:9Q24RAI43V)	VIOLA TRICOLOR	12 [hp_X] in 59 mL
ZINC BROMIDE (UNII: OO7ZBU9703) (ZINC CATION - UNII:13S1S8SF37)	ZINC BROMIDE	6 [hp_X] in 59 mL

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

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:66096-192-05	59 mL in 1 PACKAGE; Type 0: Not a Combination Product	05/22/2015

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
unapproved homeopathic		05/22/2015

Labeler - OHM PHARMA INC. (030572478)

Registrant - OHM PHARMA INC. (030572478)

Name	Address	ID/FEI	Business Operations
Establishment
OHM PHARMA INC.		030572478	manufacture(66096-192)

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