FDA label 25a84a88-1fbe-2660-e063-6394a90a1453

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
7dac9cb4-dd6a-490e-9b53-e10c2363b352
SPL ID
25a84a88-1fbe-2660-e063-6394a90a1453
Version
7
Effective date
2024-10-29
Source export date
2026-09-28
Source partition
8
Source file
https://download.open.fda.gov/drug/label/drug-label-0008-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-09-28/ae3816359e336a5de4f44607730a3d12ceb61ffa012a132189ceda22541b38ee/drug-label-0008-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 05:53:34

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 and flame Does not contain grain alcohol;do not drink. If taken internally serious gastric disturbances will result. When using this product Avoid the eyes and mucous membranes In the case of eyes or mucous membranes contact, rinse area thoroughly with water In case of deep or punture wounds or serious burns, consult physician. If redness,irritation,swelling, or pain persists or increases or if infection occurs discontinue use and consult physician. Keep out of reach of children If swallowed,contact a doctor or Poison Control Center immediately

Reported adverse events (FAERS/openFDA)#

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