FDA label 27d4f30f-0d70-5e05-e063-6394a90a534e

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
26ce6127-c90e-4c96-85b9-1a4560c5f144
SPL ID
27d4f30f-0d70-5e05-e063-6394a90a534e
Version
3
Effective date
2024-11-26
Source export date
2026-09-28
Source partition
13
Source file
https://download.open.fda.gov/drug/label/drug-label-0013-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-09-28/e78bf8aa9f90ab13e640d254dfbd4fe5bfeca4995ec5f9d51bce3356e249cab7/drug-label-0013-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 06:38:38

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 Use only as direacted Do not allow contact with the eyes and mucuous membrances. Do not apply to wounds or damaged skin Do not use at the same time as other topical analgesics Stop use and ask a doctor if : allergic reaction occurs condition worsen or does not improve within 7 days redness, irritation, swelling, pain or other symptoms begin or increase. If pregnant or Breastfeeding Ask a health professional before use. Keep out of reach of children If swallowed, get medical help or Contact a Posion Control right away. Emergency number : 1-800-222-1222

Reported adverse events (FAERS/openFDA)#

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