FDA label fe7fb301-bea0-4b20-85d4-cd22806bd46b

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
e207db09-3fe0-47ca-89b7-3a45da2cb473
SPL ID
fe7fb301-bea0-4b20-85d4-cd22806bd46b
Version
2
Effective date
2019-09-04
Source export date
2026-09-28
Source partition
10
Source file
https://download.open.fda.gov/drug/label/drug-label-0010-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-09-28/4bbc9760f647649b787710953d978bd6419e899ba8b90f32c3d972aae43947f8/drug-label-0010-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 06:11:16

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 Warnings: 1. Stop using and see a doctor in case of suffering from any adverse side effects or skin irritation as follows while using this product. a)Red spots, edema, itchy sensations, etc., while using. b)In case of having above symptoms due to direct sunlight. Do not place the product directly onto irritated or sunburned skin. 2. Do not use on spots affected by dermatitis and wounds. 3. Do not apply in case of having severe allege reaction to wear sticking plaster or wet patches. 4. Be careful not to get it in your eyes. 5. Cautions for storage and use. a) Use immediately after opening. b) Keep out of reach of children. c) Avoid prolonged exposure to extreme heat or cold and direct sunlight. d) Do not reuse.

Reported adverse events (FAERS/openFDA)#

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