NEUTROGENA SKIN CLEARING BLEMISH CONCEALER - BUFF 09- salicylic acid cream
NEUTROGENA SKIN CLEARING BLEMISH CONCEALER - FAIR 05- salicylic acid cream
NEUTROGENA SKIN CLEARING BLEMISH CONCEALER - LIGHT 10- salicylic acid cream
NEUTROGENA SKIN CLEARING BLEMISH CONCEALER - MEDIUM 15- salicylic acid cream
Johnson & Johnson Consumer Inc.

----------

Neutrogena® Skin Clearing Blemish Concealer

Drug Facts

Active ingredient

Salicylic Acid 0.5%

Purpose

Acne medication

Use

For the treatment of acne.

Warnings

For external use only.

When using this product

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.

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

Directions

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

Store at room temperature.

Inactive ingredients

Water, cyclopentasiloxane, dimethicone, kaolin, cyclomethicone, VP/hexadecene copolymer, synthetic wax, cetyl PEG/PPG-10/1 dimethicone, trisiloxane, BIS-PEG/PPG-14/14 dimethicone, cyclohexasiloxane, butylene glycol, silica, phenoxyethanol, boron nitride, polysilicone-11, quaternium-90 bentonite, sodium chloride, magnesium sulfate, propylene glycol, methylparaben, farnesol, chamomilla recutita (matricaria) flower extract, propylene carbonate, triethoxycaprylylsilane, propylparaben, aloe barbadensis leaf juice, polymethyl methacrylate, tocopheryl acetate, cocamidopropyl PG-dimonium chloride phosphate, cetyl lactate, C12-15 alkyl lactate, benzalkonium chloride, retinyl palmitate, pantothenic acid, ascorbic acid May Contain: titanium dioxide, iron oxides

Questions?

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

Dist. by
Neutrogena Corporation
Los Angeles, CA 90045

PRINCIPAL DISPLAY PANEL - 1.4 g Applicator Blister Pack - Buff 09

Buff 09
SkinClearing
blemish concealer
Don't just
cover up.
Clear up!
powered by
MICRO CLEAR®
------technology---------
Blemish
treatment
with
Salicylic
Acid

Conceals
and treats
blemishes

Natural-
looking
coverage

Neutrogena

NET WT
0.05 OZ.
(1.4g)

PRINCIPAL DISPLAY PANEL - 1.4 g Applicator Blister Pack - Buff 09

PRINCIPAL DISPLAY PANEL - 1.4 g Applicator Blister Pack - Fair 05

FAIR
05

SkinClearing
blemish concealer
Don't just
cover up.
Clear up!
powered by
MICRO CLEAR®
------technology---------
Blemish
treatment
with
Salicylic
Acid

Conceals
and treats
blemishes

Natural-
looking
coverage

Neutrogena

NET WT
0.05 OZ.
(1.4g)

PRINCIPAL DISPLAY PANEL - 1.4 g Applicator Blister Pack - Fair 05

PRINCIPAL DISPLAY PANEL - 1.4 g Applicator Blister Pack - Light 10

LIGHT
10

SkinClearing
blemish concealer
Don't just
cover up.
Clear up!
powered by
MICRO CLEAR®
------technology---------
Blemish
treatment
with
Salicylic
Acid

Conceals
and treats
blemishes

Natural-
looking
coverage

Neutrogena

NET WT
0.05 OZ.
(1.4g)

PRINCIPAL DISPLAY PANEL - 1.4 g Applicator Blister Pack - Light 10

PRINCIPAL DISPLAY PANEL - 1.4 g Applicator Blister Pack - Medium 15

MEDIUM
15

SkinClearing
blemish concealer
Don't just
cover up.
Clear up!
powered by
MICRO CLEAR®
------technology---------
Blemish
treatment
with
Salicylic
Acid

Conceals
and treats
blemishes

Natural-
looking
coverage

Neutrogena

NET WT
0.05 OZ.
(1.4g)

PRINCIPAL DISPLAY PANEL - 1.4 g Applicator Blister Pack - Medium 15

NEUTROGENA SKIN CLEARING BLEMISH CONCEALER - BUFF 09
salicylic acid cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:10812-520
Route of Administration	TOPICAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ)	SALICYLIC ACID	5.5 mg in 1 g

Ingredient Name	Strength
Inactive Ingredients
CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)
DIMETHICONE (UNII: 92RU3N3Y1O)
KAOLIN (UNII: 24H4NWX5CO)
CYCLOMETHICONE (UNII: NMQ347994Z)
VINYLPYRROLIDONE/HEXADECENE COPOLYMER (UNII: KFR5QEN0N9)
CETYL PEG/PPG-10/1 DIMETHICONE (HLB 5) (UNII: 035JKJ76MT)
TRISILOXANE (UNII: 9G1ZW13R0G)
BIS-PEG/PPG-14/14 DIMETHICONE (UNII: X2I70H0QJE)
CYCLOMETHICONE 6 (UNII: XHK3U310BA)
BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
BORON NITRIDE (UNII: 2U4T60A6YD)
DIMETHICONE/VINYL DIMETHICONE CROSSPOLYMER (SOFT PARTICLE) (UNII: 9E4CO0W6C5)
SODIUM CHLORIDE (UNII: 451W47IQ8X)
MAGNESIUM SULFATE, UNSPECIFIED FORM (UNII: DE08037SAB)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
METHYLPARABEN (UNII: A2I8C7HI9T)
FARNESOL (UNII: EB41QIU6JL)
CHAMOMILE (UNII: FGL3685T2X)
PROPYLENE CARBONATE (UNII: 8D08K3S51E)
TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E)
PROPYLPARABEN (UNII: Z8IX2SC1OH)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
COCAMIDOPROPYL PROPYLENE GLYCOL-DIMONIUM CHLORIDE PHOSPHATE (UNII: H2KVQ74JM4)
CETYL LACTATE (UNII: A7EVH2RK4O)
C12-15 ALKYL LACTATE (UNII: GC844VRD7E)
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7)
VITAMIN A PALMITATE (UNII: 1D1K0N0VVC)
PANTOTHENIC ACID (UNII: 19F5HK2737)
WATER (UNII: 059QF0KO0R)
ASCORBIC ACID (UNII: PQ6CK8PD0R)
TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
FERRIC OXIDE RED (UNII: 1K09F3G675)

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:10812-520-01	1 in 1 BLISTER PACK	02/05/2010	08/31/2025
1		1.4 g in 1 APPLICATOR; Type 0: Not a Combination Product

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC Monograph Drug	M006	02/05/2010	08/31/2025

NEUTROGENA SKIN CLEARING BLEMISH CONCEALER - FAIR 05
salicylic acid cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:10812-519
Route of Administration	TOPICAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ)	SALICYLIC ACID	5.5 mg in 1 g

Ingredient Name	Strength
Inactive Ingredients
WATER (UNII: 059QF0KO0R)
CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)
DIMETHICONE (UNII: 92RU3N3Y1O)
KAOLIN (UNII: 24H4NWX5CO)
CYCLOMETHICONE (UNII: NMQ347994Z)
VINYLPYRROLIDONE/HEXADECENE COPOLYMER (UNII: KFR5QEN0N9)
CETYL PEG/PPG-10/1 DIMETHICONE (HLB 5) (UNII: 035JKJ76MT)
TRISILOXANE (UNII: 9G1ZW13R0G)
BIS-PEG/PPG-14/14 DIMETHICONE (UNII: X2I70H0QJE)
CYCLOMETHICONE 6 (UNII: XHK3U310BA)
BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
BORON NITRIDE (UNII: 2U4T60A6YD)
DIMETHICONE/VINYL DIMETHICONE CROSSPOLYMER (SOFT PARTICLE) (UNII: 9E4CO0W6C5)
SODIUM CHLORIDE (UNII: 451W47IQ8X)
MAGNESIUM SULFATE, UNSPECIFIED FORM (UNII: DE08037SAB)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
METHYLPARABEN (UNII: A2I8C7HI9T)
FARNESOL (UNII: EB41QIU6JL)
CHAMOMILE (UNII: FGL3685T2X)
PROPYLENE CARBONATE (UNII: 8D08K3S51E)
TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E)
PROPYLPARABEN (UNII: Z8IX2SC1OH)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
COCAMIDOPROPYL PROPYLENE GLYCOL-DIMONIUM CHLORIDE PHOSPHATE (UNII: H2KVQ74JM4)
CETYL LACTATE (UNII: A7EVH2RK4O)
C12-15 ALKYL LACTATE (UNII: GC844VRD7E)
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7)
VITAMIN A PALMITATE (UNII: 1D1K0N0VVC)
PANTOTHENIC ACID (UNII: 19F5HK2737)
ASCORBIC ACID (UNII: PQ6CK8PD0R)
TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
FERRIC OXIDE RED (UNII: 1K09F3G675)

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:10812-519-01	1 in 1 BLISTER PACK	02/05/2010	08/31/2025
1		1.4 g in 1 APPLICATOR; Type 0: Not a Combination Product

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC Monograph Drug	M006	02/05/2010	08/31/2025

NEUTROGENA SKIN CLEARING BLEMISH CONCEALER - LIGHT 10
salicylic acid cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:10812-521
Route of Administration	TOPICAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ)	SALICYLIC ACID	5.5 mg in 1 g

Ingredient Name	Strength
Inactive Ingredients
WATER (UNII: 059QF0KO0R)
CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)
DIMETHICONE (UNII: 92RU3N3Y1O)
KAOLIN (UNII: 24H4NWX5CO)
CYCLOMETHICONE (UNII: NMQ347994Z)
VINYLPYRROLIDONE/HEXADECENE COPOLYMER (UNII: KFR5QEN0N9)
CETYL PEG/PPG-10/1 DIMETHICONE (HLB 5) (UNII: 035JKJ76MT)
TRISILOXANE (UNII: 9G1ZW13R0G)
BIS-PEG/PPG-14/14 DIMETHICONE (UNII: X2I70H0QJE)
CYCLOMETHICONE 6 (UNII: XHK3U310BA)
BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
BORON NITRIDE (UNII: 2U4T60A6YD)
DIMETHICONE/VINYL DIMETHICONE CROSSPOLYMER (SOFT PARTICLE) (UNII: 9E4CO0W6C5)
SODIUM CHLORIDE (UNII: 451W47IQ8X)
MAGNESIUM SULFATE, UNSPECIFIED FORM (UNII: DE08037SAB)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
METHYLPARABEN (UNII: A2I8C7HI9T)
FARNESOL (UNII: EB41QIU6JL)
CHAMOMILE (UNII: FGL3685T2X)
PROPYLENE CARBONATE (UNII: 8D08K3S51E)
TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E)
PROPYLPARABEN (UNII: Z8IX2SC1OH)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
COCAMIDOPROPYL PROPYLENE GLYCOL-DIMONIUM CHLORIDE PHOSPHATE (UNII: H2KVQ74JM4)
CETYL LACTATE (UNII: A7EVH2RK4O)
C12-15 ALKYL LACTATE (UNII: GC844VRD7E)
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7)
VITAMIN A PALMITATE (UNII: 1D1K0N0VVC)
PANTOTHENIC ACID (UNII: 19F5HK2737)
ASCORBIC ACID (UNII: PQ6CK8PD0R)
TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
FERRIC OXIDE RED (UNII: 1K09F3G675)

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:10812-521-01	1 in 1 BLISTER PACK	02/05/2010	08/31/2025
1		1.4 g in 1 APPLICATOR; Type 0: Not a Combination Product

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC Monograph Drug	M006	02/05/2010	08/31/2025

NEUTROGENA SKIN CLEARING BLEMISH CONCEALER - MEDIUM 15
salicylic acid cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:10812-522
Route of Administration	TOPICAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ)	SALICYLIC ACID	5.5 mg in 1 g

Ingredient Name	Strength
Inactive Ingredients
TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
FERRIC OXIDE RED (UNII: 1K09F3G675)
WATER (UNII: 059QF0KO0R)
CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)
DIMETHICONE (UNII: 92RU3N3Y1O)
KAOLIN (UNII: 24H4NWX5CO)
CYCLOMETHICONE (UNII: NMQ347994Z)
VINYLPYRROLIDONE/HEXADECENE COPOLYMER (UNII: KFR5QEN0N9)
CETYL PEG/PPG-10/1 DIMETHICONE (HLB 5) (UNII: 035JKJ76MT)
TRISILOXANE (UNII: 9G1ZW13R0G)
BIS-PEG/PPG-14/14 DIMETHICONE (UNII: X2I70H0QJE)
CYCLOMETHICONE 6 (UNII: XHK3U310BA)
BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
BORON NITRIDE (UNII: 2U4T60A6YD)
DIMETHICONE/VINYL DIMETHICONE CROSSPOLYMER (SOFT PARTICLE) (UNII: 9E4CO0W6C5)
SODIUM CHLORIDE (UNII: 451W47IQ8X)
MAGNESIUM SULFATE, UNSPECIFIED FORM (UNII: DE08037SAB)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
METHYLPARABEN (UNII: A2I8C7HI9T)
FARNESOL (UNII: EB41QIU6JL)
CHAMOMILE (UNII: FGL3685T2X)
PROPYLENE CARBONATE (UNII: 8D08K3S51E)
TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E)
PROPYLPARABEN (UNII: Z8IX2SC1OH)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
COCAMIDOPROPYL PROPYLENE GLYCOL-DIMONIUM CHLORIDE PHOSPHATE (UNII: H2KVQ74JM4)
CETYL LACTATE (UNII: A7EVH2RK4O)
C12-15 ALKYL LACTATE (UNII: GC844VRD7E)
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7)
VITAMIN A PALMITATE (UNII: 1D1K0N0VVC)
PANTOTHENIC ACID (UNII: 19F5HK2737)
ASCORBIC ACID (UNII: PQ6CK8PD0R)

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:10812-522-01	1 in 1 BLISTER PACK	02/05/2010	12/31/2024
1		1.4 g in 1 APPLICATOR; Type 0: Not a Combination Product

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC Monograph Drug	M006	02/05/2010	12/31/2024

Labeler - Johnson & Johnson Consumer Inc. (118772437)

Revised: 7/2024

Document Id: 1d6cdbf1-b6cb-4566-e063-6294a90ad543

Set id: 7720ebbc-522a-4398-8de6-e5a2b93ba9cb

Version: 8

Effective Time: 20240717

Johnson & Johnson Consumer Inc.