KALI PHOS

openFDA label record#

This page contains supplementary openFDA label data. For the canonical label presentation, use the corresponding DailyMed Structured Product Label.

Verified complete openFDA source JSON (canonical bytes are SHA-256 checked before publication)

Brand name: KALI PHOS
Generic name: POTASSIUM PHOSPHATE, UNSPECIFIED FORM
Manufacturer: Hyland's Inc.
Product type: HUMAN OTC DRUG
SPL set ID: ac05b704-5a09-4cfb-85ba-27f69b8a19f3
SPL ID: f032850d-4fae-2cc2-e053-2a95a90a4c96
Version: 4
Effective date: 2022-12-19
Source export date: 2026-09-28
Source partition: 11
Source file: https://download.open.fda.gov/drug/label/drug-label-0011-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-09-28/aa96b5a2be6b394393acd0090f6948bdf99e0e8e00666f81608929c8fa83db77/drug-label-0011-of-0014.json.zip
Source manifest SHA-256: cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run: 20260929T050834Z
Imported at: 2026-09-29 06:19:56

Harmonized routes table
Harmonized routes
ORAL

Harmonized identifier links#

Every typed identifier imported from the complete openFDA harmonization object is paginated here; values are not reduced to a first match.

Harmonized identifiers page 1 of 1 · 11 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
brand name		KALI PHOS	openfda.brand_name
generic name		POTASSIUM PHOSPHATE, UNSPECIFIED FORM	openfda.generic_name
manufacturer name		Hyland's Inc.	openfda.manufacturer_name
ndc	package	54973-5228-1	openfda.package_ndc
ndc	package	54973-5228-2	openfda.package_ndc
ndc	product	54973-5228	openfda.product_ndc
ndc11	package	54973522802	derived:openfda.package_ndc
ndc11	package	54973522801	derived:openfda.package_ndc
spl id		f032850d-4fae-2cc2-e053-2a95a90a4c96	id
spl set id		ac05b704-5a09-4cfb-85ba-27f69b8a19f3	set_id
unii		B7862WZ632	openfda.unii

Warnings cross-check#

openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.

Warnings sections page 1 of 1 · 1 matching rows.

warnings

Warnings Do not use if imprinted cap band is broken or missing. If symptoms persist for more than 7 days or worsen, contact a licensed health care provider. If you are pregnant or nursing, seek the advice of a licensed health care provider before using this product. Keep all medications out of the reach of children.

Reported adverse events (FAERS/openFDA)#

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