FDA.reportPublic FDA data

FDA label 0cd9629f-694b-1c5e-e063-6294a90ab388

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
0cd964a4-5983-1102-e063-6294a90a8254
SPL ID
0cd9629f-694b-1c5e-e063-6294a90ab388
Version
1
Effective date
2023-12-19
Source export date
2026-11-06
Source partition
9
Source file
https://download.open.fda.gov/drug/label/drug-label-0009-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-11-06/5731a8c92e1c0dd2a09d2f92b410e7a70ea29cbf6b8040a6a05e4be5b7c51f0d/drug-label-0009-of-0014.json.zip
Source manifest SHA-256
4a7570ba105b5a039a8e1c94a85e7f085b9047a8882a35a96bf1e4516c5ffc97
Import run
20261108T063105Z
Imported at
2026-11-08 07:44:12

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 This product is for external use, prohibit oral use. Do not use Skin ulcers, breaks and infections are prohibited. When using this product A small number of people have a mild local itching sensation during the use of the product, which does not affect the continued use of the product and can gradually disappear after stopping the use of the product. Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away. This product is a daily health product and cannot replace drugs and medical devices.

Reported adverse events (FAERS/openFDA)#

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