KALI IODATUM 1X- kali iodatum. liquid

Kali Iodatum 1X by

Drug Labeling and Warnings

Kali Iodatum 1X 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 INGREDIENT (HPUS*): Kali Iodatum 1X.

*​The letters "HPUS" indicate that the component in this product is officially monographed in the Homeopathic Pharmacopeia of the United States.

INDICATIONS & USAGE

USES: Temporarily relieves dysfunctional thyroid metabolism.**

**This statement has not been evaluated by the FDA. It is based on documented Homeopathic Materia Medica.

WARNINGS

WARNINGS: THIS PRODUCT CONTAINS IODIDE. DO NOT TAKE IF YOU ARE HIPERSENSITIVE OR ALLERGIC TO IODIDE. IF YOU ARE 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 over 12 years of age: add 1 drop (3.83 mg iodide and 1.18 mg Potassium) to 1 oz of purified water. Take 1 times per day or as directed by a health care professional. Children under 12: contact a doctor.

OTHER SAFETY INFORMATION

Do not use if cap seal is broken.

INACTIVE INGREDIENT

INACTIVE INGREDIENTS: Ethanol Alcohol 5% (Non-GMO, Kosher Certified, Corn, Gluten Allergen Free), Glycerin, Purified Water.

QUESTIONS

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

www.ohmpharma.com

PRINCIPAL DISPLAY PANEL

HOMEOPATHIC MEDICINE

NDC: 66096-166-02

KALI IODATUM 1X

Natural - Safe - Effective

No Side Effects

1 fl oz (30mL) / 5% Alcohol

PRODUCT OF USA

Temporarily relieves dysfunctional thyroid metabolism.

INGREDIENTS AND APPEARANCE

KALI IODATUM 1X 
kali iodatum. liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 66096-166
Route of Administration	ORAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
POTASSIUM IODIDE (UNII: 1C4QK22F9J) (IODIDE ION - UNII:09G4I6V86Q)	IODIDE ION	1 [hp_X]  in 30 mL

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

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 66096-166-02	30 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product	02/10/2016

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved homeopathic		02/10/2016

Labeler - OHM PHARMA INC. (030572478)

Registrant - OHM PHARMA INC. (030572478)

Establishment
Name	Address	ID/FEI	Business Operations
OHM PHARMA INC.		030572478	manufacture(66096-166)