Phosphorus 200ck

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
Phosphorus 200ck
Generic name
PHOSPHORUS
Manufacturer
SEVENE USA
Product type
HUMAN OTC DRUG
SPL set ID
cf891fd7-4546-ed1c-e053-2a95a90a471c
SPL ID
2ddc6261-f3c5-fd95-e063-6394a90a26a0
Version
4
Effective date
2025-02-11
Source export date
2026-11-06
Source partition
8
Source file
https://download.open.fda.gov/drug/label/drug-label-0008-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-11-06/db89d5ebfc3e02f44e8769334d799cd3436b05f779823ab00297f1f800c89ddf/drug-label-0008-of-0014.json.zip
Source manifest SHA-256
4a7570ba105b5a039a8e1c94a85e7f085b9047a8882a35a96bf1e4516c5ffc97
Import run
20261108T063105Z
Imported at
2026-11-08 07:33:14
Harmonized routes table
Harmonized routes
SUBLINGUAL

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 Stop use and ask a physician if symptoms persist for more than 3 days or worsen.

Reported adverse events (FAERS/openFDA)#

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