FDA label bbb36937-2b3f-aa2c-e053-2a95a90ac1eb

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
bad5f763-74da-ee72-e053-2a95a90a34ce
SPL ID
bbb36937-2b3f-aa2c-e053-2a95a90ac1eb
Version
2
Effective date
2021-02-19
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 06:30:09

Warnings cross-check#

openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.

Warnings sections page 1 of 1 · 2 matching rows.

warnings

Warnings For external use only Warnings

warnings and cautions

Other Warnings Avoid Contact with eyes. other warning Stop use and ask a doctor if: condition worsens, or if symptoms persist for more than 7 days or clear up and occur again within a few days. Stop use Pregnancy/breast-feeding warning If pregnant or breast-feeding, as a health care professional before use. Do not use in large quantity, particularly over raw surfaces or areas with blisters. do not use

Reported adverse events (FAERS/openFDA)#

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