KALI PHOSPHORICUM

Manufacturer: Washington Homeopathic Products
Effective date: 2018-06-04
Label type: HUMAN OTC DRUG LABEL
Version: 1
Source: legacy-cache
Hydrated at: 2026-08-02 00:55:13

Label at a glance#

ProductKALI PHOSPHORICUM

Active ingredientDIBASIC POTASSIUM PHOSPHATE

Label structure9 sections

Indications and uses

Irritability Weakness

Dosage and administration

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.

Label contents#

Full prescribing information#

ACTIVE INGREDIENTS

OTC - ACTIVE INGREDIENT SECTION

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

OTC - PURPOSE SECTION

Irritability
Weakness

KEEP OUT OF REACH OF CHILDREN

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

INDICATIONS

INDICATIONS & USAGE SECTION

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

WARNINGS SECTION

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

DIRECTIONS

DOSAGE & ADMINISTRATION SECTION

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

INACTIVE INGREDIENT SECTION

Lactose, Magnesium Stearate, Sodium Starch Glycolate

DO NOT USE

OTC - DO NOT USE SECTION

Do not use if seal is broken.

PRINCIPAL DISPLAY PANEL

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

KALI PHOSPHORICUM 6X

BOX

LABEL

Product Linked Resources#

Resource, Code type, Value table
Resource	Code type	Value	Equivalent identifiers	Source image
Barcode	EAN-13	0740640641958	GTIN-13: 0740640641958 EAN-13: 0740640641958 GTIN-12: 740640641958 UPC-A: 740640641958 GTIN storage (14 digits): 00740640641958	KALI PHOSPHORICUM-box.jpg

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
71919-746-36	2022-03-25	C162847	48780-1	9d75b9d0-7f3f-f424-e053-dadaa90a57ce	KALI PHOSPHORICUM
71919-746-36	2020-01-31	C162847	48780-1	9d75b9d0-7f3f-f424-e053-dadaa90a57ce	KALI PHOSPHORICUM

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 6 matching rows.

KALI PHOSPHORICUM
DIBASIC POTASSIUM PHOSPHATE
SODIUM STARCH GLYCOLATE TYPE A CORN
MAGNESIUM STEARATE
LACTOSE
POTASSIUM CATION

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
71919-746	71919-746-36

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 4 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
SODIUM STARCH GLYCOLATE TYPE A CORN	AG9B65PV6B	IACT
MAGNESIUM STEARATE	70097M6I30	IACT
LACTOSE	J2B2A4N98G	IACT
DIBASIC POTASSIUM PHOSPHATE	CI71S98N1Z	ACTIB

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
db0c054d-fdcc-16ed-e053-2995a90a7bf7			6dcae75e-a7fd-940e-e053-2a91aa0acd0c	2022-03-25	Warnings	Exact identifier spl set id: 6dcae75e-a7fd-940e-e053-2a91aa0acd0c

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.