FDA.reportPublic FDA data

FDA label ad12f690-e547-7216-e053-2a95a90aaa53

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
ad12f690-e546-7216-e053-2a95a90aaa53
SPL ID
ad12f690-e547-7216-e053-2a95a90aaa53
Version
1
Effective date
2020-08-18
Source export date
2026-09-28
Source partition
5
Source file
https://download.open.fda.gov/drug/label/drug-label-0005-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-09-28/9839785a692b692224cd5f90f9e3a9514c9923a6f521ab83eed3bedc7c0e1d05/drug-label-0005-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 05:31:20

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 Dose not contain grain alcohol; do not drink. If taken internally will produce serious gastric disturbances. When using this product When using this product Aviod the eyes and mucous membrances In the case of eyes and mucous membrances contact, rinse area thoroughly with water Stop use and ask a doctor if Stop use and ask a doctor if Condition worsens Redness or irritation develops If condition persists for more than 3 days Keep out of reach of children 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.