FDA.reportPublic FDA data

Super-Sulfur Magic Mask

Manufacturer
Starface World, Inc.
Effective date
2023-12-01
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-01 21:19:24

Label at a glance#

ProductSuper-Sulfur Magic Mask
Active ingredientSULFUR
Label structure6 sections

Indications and uses

For the treatment and management of acne. Clears up active acne blemishes and blackheads. Helps to prevent new acne blemishes and blackheads.

Dosage and administration

Clean skin. Apply to affected areas of face. Allow mask to dry for 10-15 minutes and rinse thoroughly with water to remove. Pat dry. Apply 2-3 times per week. If bothersome dryness or peeling occurs, reduce frequency of application.

Label contents#

Full prescribing information#

Active Ingredients

OTC - ACTIVE INGREDIENT SECTION

Sulfur 10%

Purpose

OTC - PURPOSE SECTION

Acne Treatment

Uses:

INDICATIONS & USAGE SECTION

For the treatment and management of acne. Clears up active acne blemishes and blackheads. Helps to prevent new acne blemishes and blackheads.

Warnings

WARNINGS SECTION

For external use only.

When using this product

OTC - WHEN USING SECTION

Skin irritattion and dryness if more likely to occur if you use another topical acne medication at the same time. If irritation occurs, only use one topical acne medication at a time.

Do not use on 

OTC - DO NOT USE SECTION

broken skin.

When using this product

OTC - WHEN USING SECTION

Apply only to areas with acne. If excessive skin irritation develops or increases, discontinue use and consult a doctor. Avoid contact with eyes and mouth.

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, get medical help or contact a Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

Clean skin. Apply to affected areas of face. Allow mask to dry for 10-15 minutes and rinse thoroughly with water to remove. Pat dry. Apply 2-3 times per week. If bothersome dryness or peeling occurs, reduce frequency of application.

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water/Aqua, Kaolin, Propanediol, Caprylic/Capric Triglyceride, Glycerin, Magnesium Aluminum Silicate, Arachidyl Alcohol, Behenyl Alcohol, Zinc Oxide, Arachidyl Glucoside, 1.2-Hexanediol, Caprylyl Glycol, Citric Acid, Vaccinium Myrtillus Leaf Cell Extract, Glucose May Contain: Ultramarines CI 77007

Package Labeling:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Outer Package2Outer Package2Inner Package2Inner Package2

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
83171-002SUPER-SULFUR MAGIC MASK (SULFUR) PASTE [STARFACE WORLD, INC.]2Unmatched20231202_09d100e8-5e04-4a96-acbd-1bd5141ecebe.zip

Products#

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

DailyMed product names page 1 of 1 · 17 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
83171-00283171-002-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 16 matching rows.

Name, UNII, Kind table
NameUNIIKind
WATER059QF0KO0RIACT
KAOLIN24H4NWX5COIACT
PROPANEDIOL5965N8W85TIACT
MEDIUM-CHAIN TRIGLYCERIDESC9H2L21V7UIACT
GLYCERINPDC6A3C0OXIACT
MAGNESIUM ALUMINUM SILICATE6M3P64V0NCIACT
ARACHIDYL ALCOHOL1QR1QRA9BUIACT
DOCOSANOL9G1OE216XYIACT
ZINC OXIDESOI2LOH54ZIACT
ARACHIDYL GLUCOSIDE6JVW35JOOJIACT
1,2-HEXANEDIOLTR046Y3K1GIACT
CAPRYLYL GLYCOL00YIU5438UIACT
CITRIC ACID MONOHYDRATE2968PHW8QPIACT
ANHYDROUS DEXTROSE5SL0G7R0OKIACT
VACCINIUM MYRTILLUS LEAFY4U591OU70IACT
SULFUR70FD1KFU70ACTIB

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
3e8ab933-99be-bfee-e063-6294a90a48cd09d100e8-5e04-4a96-acbd-1bd5141ecebe2025-09-11WarningsExact identifier
spl set id: 09d100e8-5e04-4a96-acbd-1bd5141ecebe

Reported adverse events (FAERS/openFDA)#

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