FDA label 1d56cbbb-9e8b-48d7-a34a-d7045b545fc7

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
66eb854f-12b4-4d45-ad58-199cb9259443
SPL ID
1d56cbbb-9e8b-48d7-a34a-d7045b545fc7
Version
4
Effective date
2017-08-21
Source export date
2026-09-28
Source partition
4
Source file
https://download.open.fda.gov/drug/label/drug-label-0004-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-09-28/c7ca0b7091cdaeab3f27713a6eef00adcf8fe722383633ddce61531b4c840544/drug-label-0004-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 05:22:24

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 Avoid eye contact. If contact occurs rinse thoroughly with water. In case of accidental ingestion, get medical help or contact Poison Control Center immediately Directions: pump foam into hands, lather vigorously and rinse. water, sodium Laureth Sulfate, Dipropylene glycol, glycerin, sodium PCA, Ammonium Lauryl Sulfate, cocamidopropyl betaine, polyquaternium 10, fragrance, disodium phosphate, citric acid, FD&C Yellow No. 5

Reported adverse events (FAERS/openFDA)#

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