FDA.reportPublic FDA data

87308-010

Manufacturer
Shenzhen Hengdasheng Technology Co., Ltd
Effective date
2026-07-14
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
daily-update
Hydrated at
2026-07-18 05:10:14

Label at a glance#

ProductAcne patches
Active ingredientSALICYLIC ACID
Label structure12 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 a new patch as needed.

Storage and handling

Store in a cool, dry place.

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Salicylic Acid 1%

OTC - PURPOSE SECTION

Acne Treatment

Uses

INDICATIONS & USAGE SECTION

For the treatment of acne.

Warnings

WARNINGS SECTION

For external use only.

OTC - DO NOT USE SECTION

On irritated or sunburnt skin.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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 a new patch as needed.

Other information

STORAGE AND HANDLING SECTION

Store in a cool, dry place.

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Cellulose Gum, Centella Asiatica Extract, Cyclodextrin, HydrogenatedPoly(C6-14 Olefin),Hydrogenated Polyisobutene, HydrogenatedStyrene/lsoprene Copolymer, Melaleuca Alternifolia (Tea Tree) Leaf Oil,Pentaerythrityl Tetra-Di-T-Butyl Hydroxyhydrocinnamate. Polyisobutene

OTC - WHEN USING SECTION

Using other topical acne medications at the same time or immediatelyfollowing use of this product may increase dryness or irritation of theskin. If this occurs, only one medication should be used unless directedby a doctor.· Avoid contact with eyes

OTC - STOP USE SECTION

Irritation or redness develops and persists.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

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labellabel

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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
87308-01087308-010-01

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
HYDROGENATED POLYISOBUTENE (1300 MW)7D1YQ9Y5EZIACT
HYDROGENATED POLY(C6-14 OLEFIN; 4 CST)7C6HV4SSLAIACT
CENTELLA ASIATICA7M867G6T1UIACT
POLYISOBUTYLENE (1000 MW)5XB3A63Y52IACT
MELALEUCA ALTERNIFOLIA LEAFG43C57162KIACT
CYCLODEXTRIN7E6SK9QDT8IACT
SALICYLIC ACIDO414PZ4LPZACTIB
CELLULOSE GUMK679OBS311IACT
STYRENE/ISOPRENE COPOLYMER (28:72; 210000 MW)H58HX2GWJ5IACT
PENTAERYTHRITYL TETRA-DI-T-BUTYL HYDROXYHYDROCINNAMATE255PIF62MSIACT

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
Acne patchesACNE PATCHESShenzhen Hengdasheng Technology Co., Ltd5664b9c4-6ae3-4f64-e063-6294a90a825a2026-07-14WarningsExact identifier
ndc (package): 87308-010-01
ndc (product): 87308-010
ndc11 (package): 87308001001
spl id: 569103f3-5020-a858-e063-6294a90a9ad7
spl set id: 5664b9c4-6ae3-4f64-e063-6294a90a825a

Reported adverse events (FAERS/openFDA)#

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