FDA.reportPublic FDA data

FDA label b82b6db1-f4dd-c296-e053-2a95a90a9093

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)

SPL set ID
316f6e17-d574-4c0a-bb12-aa589840d586
SPL ID
b82b6db1-f4dd-c296-e053-2a95a90a9093
Version
5
Effective date
2021-01-05
Source export date
2026-11-06
Source partition
10
Source file
https://download.open.fda.gov/drug/label/drug-label-0010-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-11-06/b0d9ca61dc485ebaf55e14a76d7d677668e40ef1e1978cdbcc4d73d58eba0b99/drug-label-0010-of-0014.json.zip
Source manifest SHA-256
4a7570ba105b5a039a8e1c94a85e7f085b9047a8882a35a96bf1e4516c5ffc97
Import run
20261108T063105Z
Imported at
2026-11-08 07:49:32

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 For external use only When using this product avoid contact with eyes. In case of eye contact, flush with water. Directions wet hands as needed lather vigorously for at least 15 seconds rinse and dry thoroughly Inactive ingredients water, sodium laureth sulfate, cocamidopropyl betaine, sodium lauryl sulfate, sodium chloride, fragrance, citric acid, PEG-150 distearate, methylchloroisothiazolinone, methylisothiazoline, FD&C yellow No. 5,D&C red No. 33

Reported adverse events (FAERS/openFDA)#

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