FDA label 0667192c-cf46-236e-e063-6294a90a57e8

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
0667192c-cf45-236e-e063-6294a90a57e8
SPL ID
0667192c-cf46-236e-e063-6294a90a57e8
Version
1
Effective date
2023-09-28
Source export date
2026-09-28
Source partition
7
Source file
https://download.open.fda.gov/drug/label/drug-label-0007-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-09-28/bb1af06e95bcf9567b07e56fcf3a03c0cac3c7c82ff89d4c970881174949e5b7/drug-label-0007-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 05:44:30

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

Precautions: 1. This product is an external product, do not take it internally; 2. This product is a health care product and does notreplace drugs and medical devices for treatment; 3. Pregnant women, infants, breastfeeding, and those allergic to this product are prohibited; 4. Do not use skin allergies, skin damage, skin diseases and other symptoms; 5. If the skin appears red, itchy and other abnormal conditions during use, please suspend use.

Reported adverse events (FAERS/openFDA)#

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