FDA.reportPublic FDA data

FDA label 79fef21c-60a7-4f4a-9dda-7d048ae6c5f8

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
122273ec-d670-4606-baf8-c9fe3fddebed
SPL ID
79fef21c-60a7-4f4a-9dda-7d048ae6c5f8
Version
4
Effective date
2014-03-27
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 07:47:54

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. Do not use on: deep puncture wounds serious burns animal bites Consult a doctor for the treatment of diaper rash. When using this product avoid contact with the eyes Stop use and ask a doctor if: condition worsens, symptoms persist for more than 7 days clears up and occurs again within a few days under 2 years of age pregnant - breast feeding Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Reported adverse events (FAERS/openFDA)#

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