Neutrogena Clear Pore Daily Scrub

Manufacturer
Johnson & Johnson Consumer Inc.
Effective date
2015-12-09
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-02 01:29:44

Label at a glance#

ProductNeutrogena Clear Pore Daily Scrub
Active ingredientBenzoyl Peroxide
Label structure11 sections

Dosage and administration

Wet Face. Squeeze into hands. Apply to face and massage gently. Rinse thoroughly. If going outside, apply sunscreen after using the product. If irritation or sensitivity develops, stop use of both products and ask a doctor.

Storage and handling

Avoid storage at extreme temperatures (below 40°F and above 100°F).

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

Drug Facts

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Benzoyl Peroxide 3.7%

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 - DO NOT USE SECTION

Do not use this medication if you

  • have very sensitive skin
  • are sensitive to benzoyl peroxide.

When using this product

OTC - WHEN USING SECTION

  • avoid unnecessary sun exposure and use sunscreen.
  • avoid contact with the eyes, lips, and mouth.
  • avoid contact with hair and dyed products, which may be bleached by this product.
  • skin irritation may occur, characterized by redness, burning, itching, peeling, or possibly swelling. Irritation may be reduced by using the product less frequently or in a lower concentration.

Stop use and ask a doctor if

OTC - STOP USE SECTION

  • irritation becomes severe.

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

Wet Face. Squeeze into hands. Apply to face and massage gently. Rinse thoroughly.

  • If going outside, apply sunscreen after using the product. If irritation or sensitivity develops, stop use of both products and ask a doctor.

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water, Glycerin, Kaolin, Bentonite, Sodium Methyl Cocoyl Taurate, Titanium Dioxide, Polyethylene, Xanthan Gum, Citric Acid, Sodium Citrate, Trideceth-9, Disodium EDTA, Fragrance, PEG-5 Ethylhexanoate, Menthol.

Questions?

OTC - QUESTIONS SECTION

Call toll-free 800-582-4084 or 215-273-8755 (collect) www.neutrogena.com

STORAGE AND HANDLING SECTION

  • Avoid storage at extreme temperatures (below 40°F and above 100°F).

SPL UNCLASSIFIED SECTION

Distributed by:
JOHNSON & JOHNSON
CONSUMER INC.

Skillman, NJ 08558

PRINCIPAL DISPLAY PANEL - 125 mL Tube Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Clear
Pore

Daily Scrub

Benzoyl Peroxide formula
penetrates pores to clear
breakout causing impurities

Neutrogena®
benzoyl peroxide acne medication
4.2 FL OZ (125mL)

PRINCIPAL DISPLAY PANEL - 125 mL Tube Label
PRINCIPAL DISPLAY PANEL - 125 mL Tube Label

Products#

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NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
69968-002769968-0027-4

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 15 matching rows.

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
ade58bb3-0501-43d1-885b-07159edab50efba9fb4d-b879-430e-b552-12bb253e05942015-12-09WarningsExact identifier
spl id: ade58bb3-0501-43d1-885b-07159edab50e
spl set id: fba9fb4d-b879-430e-b552-12bb253e0594

Reported adverse events (FAERS/openFDA)#

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