KALI MURIATICUM- potassium chloride granule

KALI MURIATICUM by

Drug Labeling and Warnings

KALI MURIATICUM by is a Homeopathic medication manufactured, distributed, or labeled by Seroyal USA, SAN’UP. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

KALI MURIATICUM 30K

PURPOSE

Indications

For the temporary relief of symptoms associated with cold and joint pain

WARNINGS

WARNING: If pregnant or breastfeeding, ask a health professional before use. Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center right away.

PREGNANCY OR BREAST FEEDING

If pregnant or breastfeeding, ask a health professional before use.

KEEP OUT OF REACH OF CHILDREN

Keep out of reach of children.

OVERDOSAGE

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

OTHER SAFETY INFORMATION

Do not use if label perforation is broken

INACTIVE INGREDIENT

INACTIVE INGREDIENTS: Lactose, sucrose

DOSAGE & ADMINISTRATION

DIRECTIONS: Adults: Take five granules three times daily or as recommended by your healthcare practitioner. Children: Take three granules and follow adult directions.

INDICATIONS & USAGE

Indications

For the temporary relief of symptoms associated with cold and joint pain

DIRECTIONS: Adults: Take five granules three times daily or as recommended by your healthcare practitioner. Children: Take three granules and follow adult directions.

PRINCIPAL DISPLAY PANEL

Homepathic Remedy

NDC: 62106-5098-4

KALI MURIATICUM

Potassium chloride

140 granules

Indications

For the temporary relief of symptoms associated with cold and joint pain

INGREDIENTS AND APPEARANCE

KALI MURIATICUM 
potassium chloride granule

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 62106-5098
Route of Administration	ORAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
POTASSIUM CHLORIDE (UNII: 660YQ98I10) (POTASSIUM CATION - UNII:295O53K152)	POTASSIUM CHLORIDE	30 [kp_C]

Inactive Ingredients
Ingredient Name	Strength
LACTOSE, UNSPECIFIED FORM (UNII: J2B2A4N98G)
SUCROSE (UNII: C151H8M554)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 62106-5098-4	10 in 1 CARTON	11/22/2018
1		140 in 1 TUBE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved homeopathic		11/22/2018

Labeler - Seroyal USA (018361118)

Establishment
Name	Address	ID/FEI	Business Operations
SAN’UP		401010287	manufacture(62106-5098)