KALI PHOSPHORICUM- dibasic potassium phosphate tablet

KALI PHOSPHORICUM by

Drug Labeling and Warnings

KALI PHOSPHORICUM by is a Homeopathic medication manufactured, distributed, or labeled by Washington Homeopathic Products. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENTS

Active ingredient (HPUS):

Kali phosphoricum 6X

The letters “HPUS” indicate that the component in this product is officially monographed in the Homeopathic Pharmacopoeia of the United States.

USES

• Irritability
• Weakness

KEEP OUT OF REACH OF CHILDREN

As with all medications, keep out of reach of children.

INDICATIONS

Indications:

Relief of symptoms of irritability and weakness.*

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

STOP USE AND ASK DOCTOR

If symptoms worsen or persist for more than 7 days, or if pregnant or nursing, consult a licensed practitioner.

DIRECTIONS

Adults: Dissolve 2-4 tablets under the tongue 3 times a day. Children: Half the adult dose. Repeat at greater intervals as condition subsides, or as directed by a licensed practitioner.

INACTIVE INGREDIENTS

Lactose, Magnesium Stearate, Sodium Starch Glycolate

DO NOT USE

Do not use if seal is broken.

PRINCIPAL DISPLAY PANEL

KALI PHOSPHORICUM 6X

INGREDIENTS AND APPEARANCE

KALI PHOSPHORICUM 
dibasic potassium phosphate tablet

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 71919-746
Route of Administration	ORAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
DIBASIC POTASSIUM PHOSPHATE (UNII: CI71S98N1Z) (POTASSIUM CATION - UNII:295O53K152)	DIBASIC POTASSIUM PHOSPHATE	6 [hp_X]

Inactive Ingredients
Ingredient Name	Strength
SODIUM STARCH GLYCOLATE TYPE A CORN (UNII: AG9B65PV6B)
MAGNESIUM STEARATE (UNII: 70097M6I30)
LACTOSE (UNII: J2B2A4N98G)

Product Characteristics
Color	white	Score	no score
Shape	ROUND	Size	5mm
Flavor		Imprint Code	None
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 71919-746-36	1 in 1 BOX	05/31/2018
1		300 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved homeopathic		05/31/2018

Labeler - Washington Homeopathic Products (084929389)

Registrant - Washington Homeopathic Products (084929389)