FDA.reportPublic FDA data

Neutrogena SkinClearing Mineral Powder - Chestnut 135

Manufacturer
Kenvue Brands LLC
Effective date
2024-11-11
Label type
HUMAN OTC DRUG LABEL
Version
7
Source
legacy-cache
Hydrated at
2026-08-01 20:49:31

Label at a glance#

ProductNeutrogena SkinClearing Mineral Powder - honey 85
Active ingredientSALICYLIC ACID
Label structure12 sections

Dosage and administration

Clean the skin thoroughly before applying this product Cover the entire affected area with a thin layer one to three times daily Because excessive drying of the skin may occur, start with one application daily, then gradually increase to two or three times daily if needed or as directed by a doctor If bothersome dryness or peeling occurs, reduce application to once a day or every other day

Storage and handling

Protect from Excessive Heat (40°C/104°F)

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

Drug Facts

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Salicylic Acid 0.5%

Purpose

OTC - PURPOSE SECTION

Acne medication

Use

INDICATIONS & USAGE SECTION

For the treatment of acne

Warnings

WARNINGS SECTION

For external use only

When using this product

OTC - WHEN USING SECTION

  • skin irritation and dryness is 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.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

  • Clean the skin thoroughly before applying this product
  • Cover the entire affected area with a thin layer one to three times daily
  • Because excessive drying of the skin may occur, start with one application daily, then gradually increase to two or three times daily if needed or as directed by a doctor
  • If bothersome dryness or peeling occurs, reduce application to once a day or every other day

Other Information

STORAGE AND HANDLING SECTION

Protect from Excessive Heat (40°C/104°F)

Inactive ingredients

INACTIVE INGREDIENT SECTION

Dimethicone, Zinc Stearate, Polyethylene, Octyldodecyl Stearoyl Stearate, C12-15 Alkyl Benzoate, Polysilicone-11, Nylon-12, Petrolatum, Ethylene/Acrylic Acid Copolymer, Calcium Silicate, Methylparaben, Sodium Dehydroacetate, Tocopheryl Acetate, Retinyl Palmitate, Propylparaben, Panthenol, Polymethyl Methacrylate, Ascorbyl Palmitate, C12-15 Alkyl Lactate, Cetyl Lactate, Benzalkonium Chloride, Cocamidopropyl PG-Dimonium Chloride Phosphate, Ascorbic Acid, Pantothenic Acid, Talc, Iron Oxides, Mica, Zinc Oxide.

May Contain: Titanium Dioxide, Carmine.

Questions ?

OTC - QUESTIONS SECTION

Call toll-free 800-480-4812 or 215-273-8755 (collect) or visit www.neutrogena.com

SPL UNCLASSIFIED SECTION

Distributed by: JOHNSON & JOHNSON CONSUMER INC.
Skillman, NJ 08558 © J&JCI 2017

PRINCIPAL DISPLAY PANEL - 11 g Container Label - Honey 85

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Neutrogena
SkinClearing ®
mineral
powder

MICRO CLEAR ®
- technology -

PRINCIPAL DISPLAY PANEL - 11 g Container Label - Honey 85
PRINCIPAL DISPLAY PANEL - 11 g Container Label - Honey 85

PRINCIPAL DISPLAY PANEL - 11 g Container Label - Chestnut 135

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Neutrogena
SkinClearing ®
mineral
powder

MICRO CLEAR ®
- technology -

PRINCIPAL DISPLAY PANEL - 11 g Container Label - Chestnut 135
PRINCIPAL DISPLAY PANEL - 11 g Container Label - Chestnut 135

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
69968-0339NEUTROGENA SKINCLEARING MINERAL POWDER - HONEY 85 (SALICYLIC ACID) CREAM NEUTROGENA SKINCLEARING MINERAL POWDER - CHESTNUT 135 (SALICYLIC ACID) CREAM [KENVUE BRANDS LLC]7Legacy NDC20241115_ab044422-db53-43de-b106-cfe1a523e4e9.zip
69968-0340NEUTROGENA SKINCLEARING MINERAL POWDER - HONEY 85 (SALICYLIC ACID) CREAM NEUTROGENA SKINCLEARING MINERAL POWDER - CHESTNUT 135 (SALICYLIC ACID) CREAM [KENVUE BRANDS LLC]7Legacy NDC20241115_ab044422-db53-43de-b106-cfe1a523e4e9.zip

Products#

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

DailyMed product names page 1 of 1 · 32 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
69968-033969968-0339-1
69968-034069968-0340-1

Ingredients#

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

DailyMed ingredient rows page 1 of 2 · 60 matching rows.

Name, UNII, Kind table
NameUNIIKind
DIMETHICONE92RU3N3Y1OIACT
TALC7SEV7J4R1UIACT
ZINC STEARATEH92E6QA4FVIACT
HIGH DENSITY POLYETHYLENEUG00KM4WR7IACT
OCTYLDODECYL STEAROYL STEARATE3D47Q6D93CIACT
MICAV8A1AW0880IACT
ALKYL (C12-15) BENZOATEA9EJ3J61HQIACT
NYLON-12446U8J075BIACT
DIMETHICONE/VINYL DIMETHICONE CROSSPOLYMER (SOFT PARTICLE)9E4CO0W6C5IACT
PETROLATUM4T6H12BN9UIACT
ACRYLIC ACID/ETHYLENE COPOLYMER (600 MPA.S)1PEZ3NLY6IIACT
CALCIUM SILICATES4255P4G5MIACT
SODIUM DEHYDROACETATE8W46YN971GIACT
METHYLPARABENA2I8C7HI9TIACT
VITAMIN A PALMITATE1D1K0N0VVCIACT
.ALPHA.-TOCOPHEROL ACETATE9E8X80D2L0IACT
PROPYLPARABENZ8IX2SC1OHIACT
PANTHENOLWV9CM0O67ZIACT
POLY(METHYL METHACRYLATE; 450000 MW)Z47NNT4J11IACT
COCAMIDOPROPYL PROPYLENE GLYCOL-DIMONIUM CHLORIDE PHOSPHATEH2KVQ74JM4IACT
CETYL LACTATEA7EVH2RK4OIACT
C12-15 ALKYL LACTATEGC844VRD7EIACT
BENZALKONIUM CHLORIDEF5UM2KM3W7IACT
ASCORBYL PALMITATEQN83US2B0NIACT
PANTOTHENIC ACID19F5HK2737IACT
ASCORBIC ACIDPQ6CK8PD0RIACT
TITANIUM DIOXIDE15FIX9V2JPIACT
FERRIC OXIDE RED1K09F3G675IACT
ZINC OXIDESOI2LOH54ZIACT
SALICYLIC ACIDO414PZ4LPZACTIB
TALC7SEV7J4R1UIACT
DIMETHICONE92RU3N3Y1OIACT
ZINC STEARATEH92E6QA4FVIACT
HIGH DENSITY POLYETHYLENEUG00KM4WR7IACT
OCTYLDODECYL STEAROYL STEARATE3D47Q6D93CIACT
MICAV8A1AW0880IACT
ALKYL (C12-15) BENZOATEA9EJ3J61HQIACT
NYLON-12446U8J075BIACT
DIMETHICONE/VINYL DIMETHICONE CROSSPOLYMER (SOFT PARTICLE)9E4CO0W6C5IACT
PETROLATUM4T6H12BN9UIACT

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
438ee539-11c5-4c5e-e063-6294a90a6b40ab044422-db53-43de-b106-cfe1a523e4e92025-11-14WarningsExact identifier
spl set id: ab044422-db53-43de-b106-cfe1a523e4e9

Reported adverse events (FAERS/openFDA)#

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