FDA label 3ec99831-f146-4691-e054-00144ff8d46c

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: 3ec99831-f145-4691-e054-00144ff8d46c
SPL ID: 3ec99831-f146-4691-e054-00144ff8d46c
Version: 1
Effective date: 2016-10-13
Source export date: 2026-10-12
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/2026-10-12/fb14b8f3d34b45230a84f851c029385f512adf3f002423a9b78d4f7ca626ecec/drug-label-0009-of-0014.json.zip
Source manifest SHA-256: 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run: 20261013T011858Z
Imported at: 2026-10-13 02:23:03

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		3ec99831-f146-4691-e054-00144ff8d46c	id
spl set id		3ec99831-f145-4691-e054-00144ff8d46c	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

For external use only When using this product 1. If any one of following symptoms occurs when using cosmetics, stop using it and consult a dermatologist. A. red spot, swelling, itching, stimulus B. symptoms mentioned above are caused by sunlight. 2. Do not apply on skin where there is wound, eczema, or irritation. 3. Storage and cautions for handling A. Close stopper after using. B. Keep out of reach of children. C. Keep away from high or low temperature and direct sunlight. 4. This is not a medicinal product. Made of 100% cosmetic ingredients, it is a sensitive-skin care product for all skin types.

Reported adverse events (FAERS/openFDA)#

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