FDA label 7c4a0160-1b29-d7b1-e053-2991aa0aa1c9

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
ad6eefe0-8f1a-4aa5-81d5-9c2daeac4fdd
SPL ID
7c4a0160-1b29-d7b1-e053-2991aa0aa1c9
Version
5
Effective date
2018-12-05
Source export date
2026-10-12
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/2026-10-12/b939c18fdf51df171cf60ce5558819d08ac66bb16bb9991d48cbec91028d783e/drug-label-0004-of-0014.json.zip
Source manifest SHA-256
7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run
20261013T011858Z
Imported at
2026-10-13 01:35:15

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 Do not get in eyes Do not apply over large areas of the body, or bandage In case of deep or puncture wounds, animal bites, or serious burns consult a doctor Stop use and ask doctor if condition worsens, or symptoms persist for more than 7 days or clear up and occur again within a few days. Do not use longer than one week unless directed by a doctor. Keep out of reach of children. If swallowed, get medical help or contact a poison control center right away. If in eyes, flush with water for 15 minutes and call a physician.

Reported adverse events (FAERS/openFDA)#

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