FDA label 64f398dc-a798-408f-e053-2a91aa0aad20

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
27d67897-429b-43c5-b395-3cb645666c31
SPL ID
64f398dc-a798-408f-e053-2a91aa0aad20
Version
2
Effective date
2017-12-01
Source export date
2026-09-28
Source partition
13
Source file
https://download.open.fda.gov/drug/label/drug-label-0013-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-09-28/e78bf8aa9f90ab13e640d254dfbd4fe5bfeca4995ec5f9d51bce3356e249cab7/drug-label-0013-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 06:34:21

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

For external use only. Do Not Use for arthritis-like conditions in children under 2. on wounds, damaged, broken or irritated skin When Using This Product use only as directed. do not bandage tightly. avoid contact with eyes or mucous membranes. Stop And Ask Doctor If condition worsens symptoms last more than 7 days symptoms clear up and com back in a few days Keep out of reach of children. If swalled get medical help or contact a Poison Control Center right away. If pregnant or breast-feeding , ask a health professional before use.

Reported adverse events (FAERS/openFDA)#

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