FDA.reportPublic FDA data

amber

Manufacturer
Pearl World Inc.
Effective date
2026-07-27
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
daily-update
Hydrated at
2026-08-06 06:10:23

Label at a glance#

Productamberglow BLEMISH PATCHES
Active ingredientSALICYLIC ACID
Label structure9 sections

Indications and uses

FOR THE TREATMENT OF ACNE.

Dosage and administration

ADULTS AND CHILDREN OVER 12 YEARS: • CLEAN AND DRY AFFECTED AREA BEFORE APPLICATION. • APPLY PATCH TO BLEMISH AND PRESS FIRMLY FOR 3-5 SECONDS. • LEAVE PATCH ON FOR UP TO 6-8 HOURS. • REMOVE AND REPLACE WITH NEW PATCH AS NEEDED.

Storage and handling

• STORE IN A COOL, DRY PLACE.

Label contents#

Full prescribing information#

ACTIVE INGREDIENT

OTC - ACTIVE INGREDIENT SECTION

SALICYLIC ACID 1%

PURPOSE

OTC - PURPOSE SECTION

ACNE TREATMENT

USES

INDICATIONS & USAGE SECTION

FOR THE TREATMENT OF ACNE.

WARNINGS

WARNINGS SECTION

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.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

KEEP OUT OF REACH OF CHILDREN.
IF INGESTED GET MEDICAL HELP OR CONTACT A POISON CONTROL CENTER RIGHT AWAY.

DIRECTIONS

DOSAGE & ADMINISTRATION SECTION

ADULTS AND CHILDREN OVER 12 YEARS:
• CLEAN AND DRY AFFECTED AREA BEFORE APPLICATION.
• APPLY PATCH TO BLEMISH AND PRESS FIRMLY FOR 3-5 SECONDS.
• LEAVE PATCH ON FOR UP TO 6-8 HOURS.
• REMOVE AND REPLACE WITH NEW PATCH AS NEEDED.

OTHER INFORMATION

STORAGE AND HANDLING SECTION

• STORE IN A COOL, DRY PLACE.

INACTIVE INGREDIENTS:

INACTIVE INGREDIENT SECTION

POLYISOBUTENE, HYDROGENATED POLY(C6-14 OLEFIN), CELLULOSE GUM, HYDROGENATED POLYISOBUTENE, HYDROGENATED STYRENE/ISOPRENE COPOLYMER, MELALEUCA ALTERNIFOLIA (TEA TREE) LEAF OIL,  PENTAERYTHRITYL TETRA-DI-T-BUTYL HYDROXYHYDROCINNAMATE, CYCLODEXTRIN, CENTELLA ASIATICA EXTRACT

SPL UNCLASSIFIED SECTION

PROTECTS BLEMISHES FROM DIRT & OIL

TEA TREE OIL INFUSED

Distributed by: Pearl World Inc. 152 W 57th St, Fl 48. NY, NY 10019
Questions or Comments call (877) 711-8333     Made in China

Packaging

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

BLEMISHPATCHES-1BLEMISHPATCHES-1

BLEMISHPATCHES-2BLEMISHPATCHES-2

BLEMISHPATCHES-3BLEMISHPATCHES-3

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 11 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
69933-72069933-720-02, 69933-720-03, 69933-720-04, 69933-720-06, 69933-720-07, 69933-720-08

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 10 matching rows.

Name, UNII, Kind table
NameUNIIKind
SALICYLIC ACIDO414PZ4LPZACTIB
POLYISOBUTYLENE (1300 MW)241BN7J12YIACT
HYDROGENATED POLY(C6-14 OLEFIN; 6 CST)3C785871IXIACT
CARBOXYMETHYLCELLULOSE SODIUM, UNSPECIFIEDK679OBS311IACT
HYDROGENATED POLYISOBUTENE (1300 MW)7D1YQ9Y5EZIACT
STYRENE/ISOPRENE/STYRENE BLOCK COPOLYMERK7S96QM8DVIACT
TEA TREE OILVIF565UC2GIACT
PENTAERYTHRITOL TETRAKIS(3-(3,5-DI-TERT-BUTYL-4-HYDROXYPHENYL)PROPIONATE)255PIF62MSIACT
CYCLODEXTRINS7E6SK9QDT8IACT
CENTELLA ASIATICA TRITERPENOIDS4YS74Q4G4JIACT

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
amberglow BLEMISH PATCHESSALICYLIC ACIDPearl World Inc.12054430-25ff-4b72-8f64-822b27abb4432026-07-27WarningsExact identifier
ndc (package): 69933-720-04
ndc (package): 69933-720-06
ndc (package): 69933-720-02
ndc (package): 69933-720-03
ndc (package): 69933-720-08
ndc (package): 69933-720-07
ndc (product): 69933-720
ndc11 (package): 69933072004
ndc11 (package): 69933072007
ndc11 (package): 69933072003
ndc11 (package): 69933072006
ndc11 (package): 69933072008
ndc11 (package): 69933072002
spl id: 5fe57cef-af01-45d7-8053-9010d262c011
spl set id: 12054430-25ff-4b72-8f64-822b27abb443

Reported adverse events (FAERS/openFDA)#

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