FDA.reportPublic FDA data

Neutrogena Blackhead Eliminating Daily Scrub

Manufacturer
Johnson & Johnson Consumer Inc.
Effective date
2023-02-28
Label type
HUMAN OTC DRUG LABEL
Version
7
Source
legacy-cache
Hydrated at
2026-08-01 21:35:24

Label at a glance#

ProductNeutrogena Blackhead Eliminating Daily Scrub
Active ingredientSALICYLIC ACID
Label structure11 sections

Dosage and administration

Cleanse twice a day. Wet face. Apply to hands, add water and work into a lather. Massage face gently. Rinse thoroughly.

Storage and handling

Store at Room Temperature.

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

Drug Facts

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Salicylic Acid 2%

Purpose

OTC - PURPOSE SECTION

Acne treatment

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.
  • avoid contact with eyes. If contact occurs, flush thoroughly with water.

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

  • Cleanse twice a day.
  • Wet face.
  • Apply to hands, add water and work into a lather.
  • Massage face gently.
  • Rinse thoroughly.

Other information

STORAGE AND HANDLING SECTION

Store at Room Temperature.

Inactive ingredients

INACTIVE INGREDIENT SECTION

water, cetyl alcohol, cellulose, PPG-15 stearyl ether, glycerin, polysorbate 60, steareth-21, potassium cetyl phosphate, xanthan gum, fragrance, disodium EDTA, menthyl lactate, sodium hydroxide, agar, iron oxides, mica, titanium dioxide, red 30

Questions?

OTC - QUESTIONS SECTION

Call toll-free 800-582-4048 or 215-273-8755 (collect). www.neutrogena.com

SPL UNCLASSIFIED SECTION

Distributed by:
JOHNSON & JOHNSON CONSUMER INC.
Skillman, NJ 08558

PRINCIPAL DISPLAY PANEL - 124 mL Tube Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Neutrogena ®

DERMATOLOGIST RECOMMENDED BRAND

Blackhead
Eliminating
daily scrub

penetrates to eliminate
most blackheads and
helps prevent new ones
gently exfoliates

salicylic acid acne treatment
4.2 FL. OZ. (124mL)

PRINCIPAL DISPLAY PANEL - 124 mL Tube Label
PRINCIPAL DISPLAY PANEL - 124 mL Tube Label

Products#

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

DailyMed product names page 1 of 1 · 19 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
69968-002569968-0025-4

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 18 matching rows.

Name, UNII, Kind table
NameUNIIKind
WATER059QF0KO0RIACT
CETYL ALCOHOL936JST6JCNIACT
POWDERED CELLULOSESMD1X3XO9MIACT
PPG-15 STEARYL ETHER1II18XLS1LIACT
GLYCERINPDC6A3C0OXIACT
POLYSORBATE 60CAL22UVI4MIACT
STEARETH-2153J3F32P58IACT
POTASSIUM CETYL PHOSPHATE03KCY6P7UTIACT
XANTHAN GUMTTV12P4NEEIACT
EDETATE DISODIUM ANHYDROUS8NLQ36F6MMIACT
MENTHYL LACTATE, (-)-2BF9E65L7IIACT
SODIUM HYDROXIDE55X04QC32IIACT
AGAR, UNSPECIFIED89T13OHQ2BIACT
FERRIC OXIDE RED1K09F3G675IACT
MICAV8A1AW0880IACT
TITANIUM DIOXIDE15FIX9V2JPIACT
D&C RED NO. 302S42T2808BIACT
SALICYLIC ACIDO414PZ4LPZACTIB

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
f5d025bc-6e95-195b-e053-2995a90ab226973dca3d-7d9b-4df8-a198-e155676a36942023-02-28WarningsExact identifier
spl id: f5d025bc-6e95-195b-e053-2995a90ab226
spl set id: 973dca3d-7d9b-4df8-a198-e155676a3694

Reported adverse events (FAERS/openFDA)#

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