FDA label 223bea3d-47ea-4c6f-8e28-454fec29981f

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
16123f22-7197-4913-8017-aa80e6f47cd9
SPL ID
223bea3d-47ea-4c6f-8e28-454fec29981f
Version
2
Effective date
2022-01-24
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 06:23:32

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 Do not use if skin is irritated or damaged excessive irritation develops 12 years of age or under When using this product avoid contact with the eyes and mucous membranes do not apply to wounds, damaged, broken or irritated skin do not bandage tightly or use a heating pad do not swallow. If swallowed, contact a physician or contact a poison control center immediately. Stop use and ask doctor if condition worses symptoms persist for more than 7 days or clear up and occur again within a few days redness develops If pregnant or breast feeding, ask a health professional before use. Keep out of reach of children.

Reported adverse events (FAERS/openFDA)#

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