KALI SULPH- potassium sulfate tablet

KALI SULPH by

Drug Labeling and Warnings

KALI SULPH by is a Homeopathic medication manufactured, distributed, or labeled by Hyland's, Standard Homeopathic Company. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

DIRECTIONS

Adults & Children ages 6 - 12: 4 tablets. Children ages 2 - 6: 2 tablets. Dissolve under tongue 3 times a day. Use more frequently (every 15 minutes for up to 8 doses) with acute conditions.

INDICATIONS

Relief of symptoms of the common cold. Relief of symptoms of pimples and blemishes associated with common acne.

FORMULA

Kali Sulphuricum 30X HPUS

in a base of Acacia Gum, Lactose N.F.

Warnings

Do not use if imprinted cap band is broken or missing.

If symptoms persist for more than seven days or worsen, contact a licensed health care provider.

Discontinue use if symptoms are accompanied by a high fever (over 101° F).

If you are pregnant or nursing, seek the advice of a licensed health care provider before using this product.

Keep this and all medications out of the reach of children.

QUESTIONS?

800.624.9659

PRINCIPAL DISPLAY PANEL - 500 Tablet Bottle Label

HOMEOPATHIC

NDC: 54973-3107-01

Hyland's®

#7

Kali Sulph. 30X

Colds,
Skin Eruptions

500 TABLETS

INGREDIENTS AND APPEARANCE

KALI SULPH 
potassium sulfate tablet

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 54973-3107
Route of Administration	ORAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
POTASSIUM SULFATE (UNII: 1K573LC5TV) (SULFATE ION - UNII:7IS9N8KPMG)	POTASSIUM SULFATE	30 [hp_X]

Inactive Ingredients
Ingredient Name	Strength
ACACIA (UNII: 5C5403N26O)
LACTOSE (UNII: J2B2A4N98G)

Product Characteristics
Color	white	Score	no score
Shape	ROUND	Size	9mm
Flavor		Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 54973-3107-1	500 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	01/01/1940
2	NDC: 54973-3107-2	1000 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	01/01/1940	12/31/2017

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved homeopathic		01/01/1940

Labeler - Hyland's (028570695)

Establishment
Name	Address	ID/FEI	Business Operations
Standard Homeopathic Company		008316655	manufacture(54973-3107) , pack(54973-3107)