Kali Sulphuricum by Ratis, LLC KALI SULPHURICUM spray

Kali Sulphuricum by

Drug Labeling and Warnings

Kali Sulphuricum by is a Homeopathic medication manufactured, distributed, or labeled by Ratis, LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT:

Kali Sulphuricum 6X 100%.

PURPOSES:

Kali Sulphuricum - tissue oxygenation, lubrication*

USES:

Temporarily helps relieve scaly skin, eczema, dandruff, hives, discolored skin, and yellow mucus from coughs and colds.*

*Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated.

WARNINGS:

For oral use only.

If pregnant or breast-feeding, ask a health care professional before use.

Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center right away.

DO NOT USE IF TAMPER EVIDENT SEAL IS BROKEN OR MISSING

KEEP OUT OF REACH OF CHILDREN:

In case of overdose, get medical help or contact a Poison Control Center right away.

DIRECTIONS:

Adults: 2 sprays 3 times a day in mouth or half a cup of water.

Children under 12: 1 spray as above.

Consult a physician for use in children under 12 years of age.

INACTIVE INGREDIENTS:

Demineralized water, 20% organic ethanol 

QUESTIONS:

www.HomeopathyStore.com

(888) 405-7551

Dist. by Ratis, LLC

1201 N Orange St

Ste 7594

Wilmington, DE 19801

PACKAGE LABEL DISPLAY:

SCHUESSLER CELL SALTS

LACTOSE FREE

ANNA

KARE

Kali

Sulphuricum

HOMEOPATHIC ORAL SPRAY

1 FL. OZ (30ML)

INGREDIENTS AND APPEARANCE

KALI SULPHURICUM 
kali sulphuricum spray

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 71753-8007
Route of Administration	ORAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
POTASSIUM SULFATE (UNII: 1K573LC5TV) (POTASSIUM CATION - UNII:295O53K152)	POTASSIUM SULFATE	6 [hp_X]  in 1 mL

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

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 71753-8007-1	30 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	09/30/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved homeopathic		09/30/2020

Labeler - Ratis, LLC (964594324)