FDA label bafb21d2-ec05-7029-e053-2995a90a399e

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
aaf5a5f2-f885-144f-e053-2995a90a30c1
SPL ID
bafb21d2-ec05-7029-e053-2995a90a399e
Version
2
Effective date
2021-02-10
Source export date
2026-10-12
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/2026-10-12/fa098e7c5cff0b1ab653ce934059d1f4b90b860bafc0383a1f66223ce1037518/drug-label-0008-of-0014.json.zip
Source manifest SHA-256
7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run
20261013T011858Z
Imported at
2026-10-13 02:08:35

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 heat and flame Does not contain grain alcohol; do not drink If taken internally will produce serious gastric disturbances When using this product Avoid the eyes and mucous membranes In the case of eyes or mucous membrane contact, rinse thoroughly with water 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. 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.