FDA.reportPublic FDA data

Neutrogena Blackhead Eliminating Cleanser Mask

Manufacturer
Johnson & Johnson Consumer Inc.
Effective date
2018-11-17
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-02 00:46:16

Label at a glance#

ProductNeutrogena Blackhead Eliminating Cleanser Mask
Active ingredientSalicylic Acid
Label structure11 sections

Dosage and administration

To use as a cleanser: Wet face. Squeeze into hands. Apply to face and massage gently. Rinse thoroughly. To use as a mask: Do not exceed two to three times per week. Squeeze into hands. Smooth an even layer over skin. Allow to dry up to five minutes. Rinse thoroughly. If excessive drying or bothersome peeling occurs, reduce application to once per week (mask use) and every other day (cleanser use).

Storage and handling

Sunburn Alert: This product contains an alpha hydroxy acid (AHA) that may increase your skin's sensitivity to the sun and particularly the possibility of sunburn. Use a sunscreen, wear protective clothing and limit sun exposure while using this product and for a week afterwards. 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 acnex` 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

  • To use as a cleanser: Wet face. Squeeze into hands. Apply to face and massage gently. Rinse thoroughly.
  • To use as a mask: Do not exceed two to three times per week. Squeeze into hands. Smooth an even layer over skin. Allow to dry up to five minutes. Rinse thoroughly.
  • If excessive drying or bothersome peeling occurs, reduce application to once per week (mask use) and every other day (cleanser use).

Other information

STORAGE AND HANDLING SECTION

  • Sunburn Alert: This product contains an alpha hydroxy acid (AHA) that may increase your skin's sensitivity to the sun and particularly the possibility of sunburn. Use a sunscreen, wear protective clothing and limit sun exposure while using this product and for a week afterwards.
  • Store at Room Temperature

Inactive ingredients

INACTIVE INGREDIENT SECTION

water, cetyl alcohol, polyethylene, PPG-15 stearyl ether, polysorbate 60, steareth-21, potassium cetyl phosphate, xanthan gum, steareth-2, C12-15 alkyl lactate, cocamidopropyl PG-dimonium chloride phosphate, fragrance, sodium hydroxide, cetyl lactate, menthyl lactate, disodium EDTA, benzalkonium chloride, citric acid, titanium dioxide

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 - 118 mL Tube Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Blackhead
Eliminating
Cleanser/Mask

MICROCLEAR®
technology

Keeps blackheads away
for up to 3 weeks

use as a    or a deep

daily                    penetrating

cleanser              mask

Neutrogena®

salicylic acid acne treatment
4 FL. OZ. (118 mL)

PRINCIPAL DISPLAY PANEL - 118 mL Tube Label
PRINCIPAL DISPLAY PANEL - 118 mL Tube Label

Products#

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

DailyMed product names page 1 of 1 · 20 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
69968-015969968-0159-4

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 19 matching rows.

Name, UNII, Kind table
NameUNIIKind
Salicylic AcidO414PZ4LPZACTIB
Water059QF0KO0RIACT
Cetyl Alcohol936JST6JCNIACT
High Density PolyethyleneUG00KM4WR7IACT
PPG-15 Stearyl Ether1II18XLS1LIACT
Steareth-2153J3F32P58IACT
Titanium Dioxide15FIX9V2JPIACT
Polysorbate 60CAL22UVI4MIACT
Potassium Cetyl Phosphate03KCY6P7UTIACT
Xanthan GumTTV12P4NEEIACT
C12-15 Alkyl LactateGC844VRD7EIACT
Steareth-2V56DFE46J5IACT
Cocamidopropyl Propylene Glycol-Dimonium Chloride PhosphateH2KVQ74JM4IACT
Sodium Hydroxide55X04QC32IIACT
Menthyl Lactate, (-)-2BF9E65L7IIACT
Cetyl LactateA7EVH2RK4OIACT
Citric Acid Monohydrate2968PHW8QPIACT
Edetate Disodium7FLD91C86KIACT
Benzalkonium ChlorideF5UM2KM3W7IACT

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
cff93afc-cf75-4482-a6ea-8dfd4be8a6cf83441a84-2e55-4b60-a53c-bb8d31cbee9c2020-06-23WarningsExact identifier
spl set id: 83441a84-2e55-4b60-a53c-bb8d31cbee9c

Reported adverse events (FAERS/openFDA)#

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