amberglow BLEMISH PATCHES

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: amberglow BLEMISH PATCHES
Generic name: SALICYLIC ACID
Manufacturer: Pearl World Inc.
Product type: HUMAN OTC DRUG
SPL set ID: 12054430-25ff-4b72-8f64-822b27abb443
SPL ID: 5fe57cef-af01-45d7-8053-9010d262c011
Version: 1
Effective date: 2026-07-27
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 06:07:46

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 · 21 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		M006	openfda.application_number
brand name		amberglow BLEMISH PATCHES	openfda.brand_name
generic name		SALICYLIC ACID	openfda.generic_name
manufacturer name		Pearl World Inc.	openfda.manufacturer_name
ndc	package	69933-720-04	openfda.package_ndc
ndc	package	69933-720-06	openfda.package_ndc
ndc	package	69933-720-02	openfda.package_ndc
ndc	package	69933-720-03	openfda.package_ndc
ndc	package	69933-720-08	openfda.package_ndc
ndc	package	69933-720-07	openfda.package_ndc
ndc	product	69933-720	openfda.product_ndc
ndc11	package	69933072004	derived:openfda.package_ndc
ndc11	package	69933072007	derived:openfda.package_ndc
ndc11	package	69933072003	derived:openfda.package_ndc
ndc11	package	69933072006	derived:openfda.package_ndc
ndc11	package	69933072008	derived:openfda.package_ndc
ndc11	package	69933072002	derived:openfda.package_ndc
rxcui		2688025	openfda.rxcui
spl id		5fe57cef-af01-45d7-8053-9010d262c011	id
spl set id		12054430-25ff-4b72-8f64-822b27abb443	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. WHEN USING THIS PRODUCT • USING OTHER TOPICAL ACNE MEDICATIONS AT THE SAME TIME OR IMMEDIATELY FOLLOWING USE OF THIS PRODUCT MAY INCREASE DRYNESS OR IRRITATION OF THE SKIN. IF THIS OCCURS, ONLY ONE MEDICATION SHOULD BE USED UNLESS DIRECTED BY A DOCTOR. • AVOID CONTACT WITH EYES. STOP USE AND ASK A DOCTOR IF • IRRITATION OR REDNESS DEVELOPS AND PERSISTS. DO NOT USE • ON IRRITATED OR SUNBURNT SKIN. KEEP OUT OF REACH OF CHILDREN. IF INGESTED GET MEDICAL HELP OR CONTACT A POISON CONTROL CENTER RIGHT AWAY.

Reported adverse events (FAERS/openFDA)#

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