FDA label c795fd69-e1ea-4163-8b40-4a1524654091

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: 7b95c957-665d-4f01-b8de-de3cfa59f1e5
SPL ID: c795fd69-e1ea-4163-8b40-4a1524654091
Version: 1
Effective date: 2014-03-02
Source export date: 2026-09-28
Source partition: 5
Source file: https://download.open.fda.gov/drug/label/drug-label-0005-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-09-28/9839785a692b692224cd5f90f9e3a9514c9923a6f521ab83eed3bedc7c0e1d05/drug-label-0005-of-0014.json.zip
Source manifest SHA-256: cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run: 20260929T050834Z
Imported at: 2026-09-29 05:30:12

Harmonized identifier links#

Every typed identifier imported from the complete openFDA harmonization object is paginated here; values are not reduced to a first match.

Harmonized identifiers page 1 of 1 · 2 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
spl id		c795fd69-e1ea-4163-8b40-4a1524654091	id
spl set id		7b95c957-665d-4f01-b8de-de3cfa59f1e5	set_id

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

A. Please stop using the product in anyone of the following cases: 1) Rash, swelling, itching, irritation, and other abnormal reactions on the skin after using the product. 2) When the abnormalities above appear on the skin due to direct sunlight, etc. B. Do NOT use on a scar, or skin affected by dermatitis, eczema, etc. C. Notes for Storage 1) Make sure to close the lid after use. 2) Keep away from babies and children. 3) Do not store in high/low temperature or under direct sun light. Abnormal products will be compensated for according to “Standard for Consumer Dispute Resolution” by Fair Trade Commission

Reported adverse events (FAERS/openFDA)#

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