FDA label 1a167923-a475-cbc7-e063-6394a90a33d0

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
61081e8e-bae8-3500-e053-2a91aa0ac312
SPL ID
1a167923-a475-cbc7-e063-6394a90a33d0
Version
11
Effective date
2024-06-04
Source export date
2026-09-28
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/2026-09-28/663999d0fe1757c1e2cd13a4799d76d875f663e0bc57701092264ebe7febfc18/drug-label-0012-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 06:23:41

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 Flammable keep away from fire or flame contents under pressure do not puncture or incinerate container do not expose to temperature above 120 0 F Do not use in the eyes or other mucous membranes in cases of serious burns in case of deep orpuncture wounds for a prolonged period of time on large portion of the body Stop use and ask a doctor if condition worsens or symptoms persist for more than 7 days condition clears up and occurs again within a few days redness, swelling, or irritation occurs 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.