Sulwhasoo Perfecting Cushion NO.21N1 Beige

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: Sulwhasoo Perfecting Cushion NO.21N1 Beige
Generic name: OCTINOXATE, TITANIUM DIOXIDE, AND HOMOSALATE
Manufacturer: Amorepacific Corporation
Product type: HUMAN OTC DRUG
SPL set ID: 3350f28e-22b4-904c-e063-6394a90a1c81
SPL ID: 3350f28e-22b5-904c-e063-6394a90a1c81
Version: 1
Effective date: 2025-04-21
Source export date: 2026-10-30
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/2026-10-30/57469fe40e5b1c0d9604dc7dbc22532ea48e8e53acfb911fc676578d98492f7e/drug-label-0002-of-0014.json.zip
Source manifest SHA-256: b11f1f6b476c7417db937215bf14307ef1a0b69465b42b411ad52f42ae36ead3
Import run: 20261102T182004Z
Imported at: 2026-11-02 18:30:18

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 · 36 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		M020	openfda.application_number
brand name		Sulwhasoo Perfecting Cushion NO.31W1 Almond	openfda.brand_name
brand name		Sulwhasoo Perfecting Cushion NO.33C1 Walnut	openfda.brand_name
brand name		Sulwhasoo Perfecting Cushion NO.23N1 Sand	openfda.brand_name
brand name		Sulwhasoo Perfecting Cushion NO.37W1 Maple	openfda.brand_name
brand name		Sulwhasoo Perfecting Cushion NO.17N1 Vanilla	openfda.brand_name
brand name		Sulwhasoo Perfecting Cushion NO.21N1 Beige	openfda.brand_name
brand name		Sulwhasoo Perfecting Cushion NO.25N1 Amber	openfda.brand_name
generic name		OCTINOXATE, TITANIUM DIOXIDE, AND HOMOSALATE	openfda.generic_name
manufacturer name		Amorepacific Corporation	openfda.manufacturer_name
ndc	package	43419-089-31	openfda.package_ndc
ndc	package	43419-091-31	openfda.package_ndc
ndc	package	43419-087-31	openfda.package_ndc
ndc	package	43419-090-31	openfda.package_ndc
ndc	package	43419-086-31	openfda.package_ndc
ndc	package	43419-092-31	openfda.package_ndc
ndc	package	43419-093-31	openfda.package_ndc
ndc	product	43419-093	openfda.product_ndc
ndc	product	43419-091	openfda.product_ndc
ndc	product	43419-090	openfda.product_ndc
ndc	product	43419-089	openfda.product_ndc
ndc	product	43419-086	openfda.product_ndc
ndc	product	43419-087	openfda.product_ndc
ndc	product	43419-092	openfda.product_ndc
ndc11	package	43419008931	derived:openfda.package_ndc
ndc11	package	43419009331	derived:openfda.package_ndc
ndc11	package	43419009131	derived:openfda.package_ndc
ndc11	package	43419009231	derived:openfda.package_ndc
ndc11	package	43419008731	derived:openfda.package_ndc
ndc11	package	43419008631	derived:openfda.package_ndc
ndc11	package	43419009031	derived:openfda.package_ndc
spl id		3350f28e-22b5-904c-e063-6394a90a1c81	id
spl set id		3350f28e-22b4-904c-e063-6394a90a1c81	set_id
unii		V06SV4M95S	openfda.unii
unii		15FIX9V2JP	openfda.unii
unii		4Y5P7MUD51	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 Do not use on broken skin. When using this product avoid contact with eyes. If contact occurs, rinse thoroughly with water. Stop use and ask a doctor if rash occurs. Keep out of reach of children . If swallowed, call a poison control centre or get medical help right away.

Reported adverse events (FAERS/openFDA)#

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