NEUTROGENA ® Rapid Clear ® Acne Defense Face Lotion

Manufacturer
Johnson & Johnson Consumer Inc.
Effective date
2020-06-02
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
legacy-cache
Hydrated at
2026-08-01 23:27:40

Label at a glance#

ProductNeutrogena Rapid Clear Acne Defense Face
Active ingredientSalicylic Acid
Label structure11 sections

Dosage and administration

cleanse 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 2%

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.
  • if eye 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 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

Water, C12-15 Alkyl Benzoate, Butylene Glycol, Cetyl Alcohol, Dimethicone, Dimethicone PEG-8 Beeswax, Glyceryl Stearate, PEG-100 Stearate, Potassium Cetyl Phosphate, Capryloyl Glycine, Hydrogenated Palm Glycerides, Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Xanthan Gum, Sarcosine, Sodium Hydroxide, Propylene Glycol, Fragrance, Tocopheryl Acetate, Cinnamomum Zeylanicum Bark Extract, Bisabolol, Allantoin, Cedrus Atlantica Bark Extract, Portulaca Oleracea Extract, Citric Acid

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 - 50 mL Tube Carton

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

NEW INFO
NEUTROGENA
Rapid
Clear™
Acne
Defense
Face Lotion

oil-free daily lotion
leaves skin soft
and smooth

visibly reduces
breakouts in
8 HOURS

helps prevent
new breakouts

Neutrogena®

salicylic acid acne treatment

1.7 FL. OZ. (50 mL)

Principal Display Panel - 50 mL Tube Carton
Principal Display Panel - 50 mL Tube Carton

Products#

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NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
69968-013169968-0131-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 22 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
56a1d819-b6b0-4b26-acf8-7dc6e3a9cb5e51f03428-f25a-4d6f-affb-71c41effd67b2020-06-02WarningsExact identifier
spl id: 56a1d819-b6b0-4b26-acf8-7dc6e3a9cb5e
spl set id: 51f03428-f25a-4d6f-affb-71c41effd67b

Reported adverse events (FAERS/openFDA)#

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