Acne Moisturizer

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)

Brand name: Acne Moisturizer
Generic name: SALICYLIC ACID
Manufacturer: Spa de Soleil
Product type: HUMAN OTC DRUG
SPL set ID: 0a9047c8-2038-7c92-e063-6294a90a5998
SPL ID: 48df0f6d-b5dc-4142-e063-6394a90a7968
Version: 3
Effective date: 2026-01-20
Source export date: 2026-10-27
Source partition: 12
Source file: https://download.open.fda.gov/drug/label/drug-label-0012-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-10-27/977776a6cc37ec1c77259da8a93ae161850a3aa120341096e5a03428b84d016b/drug-label-0012-of-0014.json.zip
Source manifest SHA-256: 6be3667a3beefe6c0ead4c723ea963050533a2bc725a8044d58b07d18b258c55
Import run: 20261027T193451Z
Imported at: 2026-10-27 20:58:54

Harmonized routes table
Harmonized routes
TOPICAL

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 · 10 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		M006	openfda.application_number
brand name		Acne Moisturizer	openfda.brand_name
generic name		SALICYLIC ACID	openfda.generic_name
manufacturer name		Spa de Soleil	openfda.manufacturer_name
ndc	package	68062-9907-1	openfda.package_ndc
ndc	product	68062-9907	openfda.product_ndc
ndc11	package	68062990701	derived:openfda.package_ndc
spl id		48df0f6d-b5dc-4142-e063-6394a90a7968	id
spl set id		0a9047c8-2038-7c92-e063-6294a90a5998	set_id
unii		O414PZ4LPZ	openfda.unii

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 For external use only Avoid contact with eyes. If contact occurs, rinse thoroughly with water. If swallowed, get medical help or contact a Poison Control Center right away. If excessive skin irritation develops or increases, discontinue use and consult a doctor. Keep out of reach of children.

Reported adverse events (FAERS/openFDA)#

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