FDA label 7d7930af-de9e-4992-b550-b8eccecfa113

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
beecd380-d8ef-4d00-8e85-08019ac1a960
SPL ID
7d7930af-de9e-4992-b550-b8eccecfa113
Version
1
Effective date
2018-10-11
Source export date
2026-11-06
Source partition
2
Source file
https://download.open.fda.gov/drug/label/drug-label-0002-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-11-06/4dafeb36642dffb72e2138939a956de402f722ea8c14c08cd87068efd3669f01/drug-label-0002-of-0014.json.zip
Source manifest SHA-256
4a7570ba105b5a039a8e1c94a85e7f085b9047a8882a35a96bf1e4516c5ffc97
Import run
20261108T063105Z
Imported at
2026-11-08 06:52:06

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 Precautions of Use 1. If rash, redness, swelling, itching or other adverse reactions occur as a result of exposure to sunlight during or after use, consult a doctor / specialist. 2. Refrain from using on wound sites. 3. Storage and handling precautions: i) Keep out of reach of children. ii) Keep away from direct sunlight 4. Avoid applying on the eye area 5. Use immediately after opening the package as the product may become dry, and do not reuse. 6. Be cautious if you have irritation on adhesive bandages and poultices.

Reported adverse events (FAERS/openFDA)#

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