FDA label b82b6db1-f4d3-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
63241c2f-55f0-4c33-8917-c9de024ba352
SPL ID
b82b6db1-f4d3-c296-e053-2a95a90a9093
Version
5
Effective date
2021-01-05
Source export date
2026-10-12
Source partition
12
Source file
https://download.open.fda.gov/drug/label/drug-label-0012-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-10-12/edd23646015c9adc800cdbe2b778398a2d2b70e90dce5721ef2b191499a0397f/drug-label-0012-of-0014.json.zip
Source manifest SHA-256
7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run
20261013T011858Z
Imported at
2026-10-13 02:49:26

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 Directions wet hands as needed lather vigorously for at least 15 seconds rinse and dry water (aqua), sodium laureth sulfate, ammonium lauryl sulfate, decyl glucoside, cocamidopropyl betaine, glycerin, sodium chloride, PEG-18 glyceryl oleate/cocoate, fragrance, DMDM hydantoin, tetrasodium EDTA, citric acid, FD&C blue 1, D&C red 33.

Reported adverse events (FAERS/openFDA)#

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