KALI PHOSPHORICUM- potassium phosphate, dibasic pellet

Kali phosphoricum by

Drug Labeling and Warnings

Kali phosphoricum by is a Homeopathic medication manufactured, distributed, or labeled by Laboratoires Boiron, Boiron Inc., Boiron. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredients

Kali phosphoricum HPUS

PURPOSE

Use

Tension Headaches Associated With Intellectual Fatigue*

Warnings

Stop use and ask a doctor if

symptoms persist for more than 3 days or worsen.

If pregnant or breast-feeding,

ask a health professional before use.

Keep out of reach of children.

Directions

5 pellets 3 times a day until symptoms are relieved.

Other information

Do not use if pellet dispenser seal is broken.
contains approx. 80 pellets

Inactive ingredients

lactose, sucrose

Questions, Comments?

1-800-BOIRON-1
Newtown Square, PA 19073-3267
info@boironusa.com

SPL UNCLASSIFIED SECTION

Do not use if pellet dispenser seal is broken.

Contains approx 80 pellets.
How to dispense pellets? Turn tube upside down. Twist until 5 pellets are dispensed into cap. Carefully remove the cap and use it to pour pellets under the tongue.
*CLAIMS BASED ON TRADITIONAL HOMEOPATHIC PRACTICE NOT ACCEPTED MEDICAL EVIDENCE. NOT FDA EVALUATED.
*C,K,CK, and X are homeopathic dilutions: see BoironUSA.com/info for details.

Principle Display Panel - Kali phosphoricum

INGREDIENTS AND APPEARANCE

KALI PHOSPHORICUM 
potassium phosphate, dibasic pellet

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 0220-2908
Route of Administration	ORAL

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

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

Product Characteristics
Color	white	Score
Shape	ROUND	Size	4mm
Flavor		Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0220-2908-41	80 in 1 TUBE; Type 0: Not a Combination Product	03/03/1983
2	NDC: 0220-2908-43	3 in 1 PACKAGE	05/15/2017
2		80 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		03/03/1983

Labeler - Laboratoires Boiron (282560473)

Registrant - Boiron Inc. (014892269)

Establishment
Name	Address	ID/FEI	Business Operations
Boiron		282560473	manufacture(0220-2908)