NEUTROGENA HEALTHY SKIN GLOW SHEERS ILLUMINATING TINTED MOISTURIZER - IVORY TO FAIR 10 SUNSCREEN BROAD SPECTRUM SPF30- homosalate, octinoxate, octisalate, oxybenzone, and titanium dioxide liquid NEUTROGENA HEALTHY SKIN GLOW SHEERS ILLUMINATING TINTED MOISTURIZER - FAIR TO LIGHT 20 SUNSCREEN BROAD SPECTRUM SPF30- homosalate, octinoxate, octisalate, oxybenzone, and titanium dioxide liquid NEUTROGENA HEALTHY SKIN GLOW SHEERS ILLUMINATING TINTED MOISTURIZER - LIGHT TO MEDIUM 30 SUNSCREEN BROAD SPECTRUM SPF30- homosalate, octinoxate, octisalate, oxybenzone, and titanium dioxide liquid

Neutrogena Healthy Skin Glow Sheers Illuminating Tinted Moisturizer - Light to Medium 30 by

Drug Labeling and Warnings

Neutrogena Healthy Skin Glow Sheers Illuminating Tinted Moisturizer - Light to Medium 30 by is a Otc medication manufactured, distributed, or labeled by Johnson & Johnson Consumer Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

SPL UNCLASSIFIED SECTION

Drug Facts

Active ingredients

Homosalate 5%, Octinoxate 7.5%, Octisalate 5%, Oxybenzone 2%, Titanium Dioxide 2.9%

Purpose

Sunscreen

Uses

• helps prevent sunburn
• if used as directed with other sun protection measures (see Directions), decreases the risk of skin cancer and early skin aging caused by the sun

Warnings

For external use only

• Do not use on damaged or broken skin

• When using this product keep out of eyes . Rinse with water to remove.

• Stop use and ask a doctor if rash occurs

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

Directions

For Sunscreen Use:

• apply liberally 15 minutes before sun exposure
• reapply at least every 2 hours
• use a water resistant sunscreen if swimming or sweating
• Sun Protection Measures: Spending time in the sun increases your risk of skin cancer and early skin aging . To decrease this risk, regularly use a sunscreen with a Broad Spectrum SPF value of 15 or higher and other sun protection measures including:
  • limit time in the sun, especially from 10 a.m. - 2 p.m.
  • wear long-sleeved shirts, pants, hats, and sunglasses
• children under 6 months of age: Ask a doctor

Other information

• protect this product from excessive heat and direct sun
• may stain some fabrics

Inactive ingredients

water, phenyl trimethicone, cetyl dimethicone, butylene glycol, silica, cetearyl alcohol, glyceryl stearate, PEG 100 stearate, barium sulfate, pantothenic acid, ascorbic acid, tocopheryl acetate, retinyl palmitate, squalane, bisabolol, dipotassium glycyrrhizate, polysorbate 60, PEG-12 dimethicone, polymethyl methacrylate, polysorbate 20, magnesium aluminum silicate, cetyl hydroxyethylcellulose, tetrasodium EDTA, xanthan gum, hydroxyethyl acrylate/sodium acryloyldimethyl taurate, caprylyl glycol, sorbic acid, phenoxyethanol May contain: iron oxides, mica, titanium dioxide

Questions?

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

SPL UNCLASSIFIED SECTION

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

PRINCIPAL DISPLAY PANEL - 32 mL Tube Label - Ivory to Fair 10

Neutrogena
healthy skin
glow sheers ®

illuminating
tinted moisturizer

with
sunscreen

broad spectrum
SPF 30

lightweight
antioxidant blend
oil-free

ivory to fair 10
1.1 FL. OZ. (32mL)

PRINCIPAL DISPLAY PANEL - 32 mL Tube Label - Fair to Light 20

Neutrogena
healthy skin
glow sheers ®

illuminating
tinted moisturizer

with
sunscreen

broad spectrum
SPF 30

lightweight
antioxidant blend
oil-free

fair to light 20
1.1 FL. OZ. (32mL)

PRINCIPAL DISPLAY PANEL - 32 mL Tube Label - Light to Medium 30

Neutrogena
healthy skin
glow sheers ®

illuminating
tinted moisturizer

with
sunscreen

broad spectrum
SPF 30

lightweight
antioxidant blend
oil-free

light to medium 30
1.1 FL. OZ. (32mL)

INGREDIENTS AND APPEARANCE

NEUTROGENA HEALTHY SKIN GLOW SHEERS ILLUMINATING TINTED MOISTURIZER - IVORY TO FAIR 10  SUNSCREEN BROAD SPECTRUM SPF30
homosalate, octinoxate, octisalate, oxybenzone, and titanium dioxide liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 69968-0116
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
HOMOSALATE (UNII: V06SV4M95S) (HOMOSALATE - UNII:V06SV4M95S)	HOMOSALATE	50 mg  in 1 mL
OCTINOXATE (UNII: 4Y5P7MUD51) (OCTINOXATE - UNII:4Y5P7MUD51)	OCTINOXATE	75 mg  in 1 mL
OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W)	OCTISALATE	50 mg  in 1 mL
OXYBENZONE (UNII: 95OOS7VE0Y) (OXYBENZONE - UNII:95OOS7VE0Y)	OXYBENZONE	20 mg  in 1 mL
TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (TITANIUM DIOXIDE - UNII:15FIX9V2JP)	TITANIUM DIOXIDE	29 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
PHENYL TRIMETHICONE (UNII: DR0K5NOJ4R)
BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
PEG-100 STEARATE (UNII: YD01N1999R)
BARIUM SULFATE (UNII: 25BB7EKE2E)
PANTOTHENIC ACID (UNII: 19F5HK2737)
ASCORBIC ACID (UNII: PQ6CK8PD0R)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
VITAMIN A PALMITATE (UNII: 1D1K0N0VVC)
SQUALANE (UNII: GW89575KF9)
LEVOMENOL (UNII: 24WE03BX2T)
GLYCYRRHIZINATE DIPOTASSIUM (UNII: CA2Y0FE3FX)
POLYSORBATE 60 (UNII: CAL22UVI4M)
PEG-12 DIMETHICONE (300 CST) (UNII: ZEL54N6W95)
POLY(METHYL METHACRYLATE; 450000 MW) (UNII: Z47NNT4J11)
POLYSORBATE 20 (UNII: 7T1F30V5YH)
MAGNESIUM ALUMINUM SILICATE (UNII: 6M3P64V0NC)
EDETATE SODIUM (UNII: MP1J8420LU)
XANTHAN GUM (UNII: TTV12P4NEE)
HYDROXYETHYL ACRYLATE/SODIUM ACRYLOYLDIMETHYL TAURATE COPOLYMER (100000 MPA.S AT 1.5%) (UNII: 86FQE96TZ4)
CAPRYLYL GLYCOL (UNII: 00YIU5438U)
SORBIC ACID (UNII: X045WJ989B)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
FERRIC OXIDE RED (UNII: 1K09F3G675)
MICA (UNII: V8A1AW0880)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 69968-0116-1	32 mL in 1 TUBE; Type 0: Not a Combination Product	05/23/2013	12/31/2023

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M020	05/23/2013	12/31/2023

NEUTROGENA HEALTHY SKIN GLOW SHEERS ILLUMINATING TINTED MOISTURIZER - FAIR TO LIGHT 20  SUNSCREEN BROAD SPECTRUM SPF30
homosalate, octinoxate, octisalate, oxybenzone, and titanium dioxide liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 69968-0115
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
OXYBENZONE (UNII: 95OOS7VE0Y) (OXYBENZONE - UNII:95OOS7VE0Y)	OXYBENZONE	20 mg  in 1 mL
TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (TITANIUM DIOXIDE - UNII:15FIX9V2JP)	TITANIUM DIOXIDE	29 mg  in 1 mL
HOMOSALATE (UNII: V06SV4M95S) (HOMOSALATE - UNII:V06SV4M95S)	HOMOSALATE	50 mg  in 1 mL
OCTINOXATE (UNII: 4Y5P7MUD51) (OCTINOXATE - UNII:4Y5P7MUD51)	OCTINOXATE	75 mg  in 1 mL
OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W)	OCTISALATE	50 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
PEG-100 STEARATE (UNII: YD01N1999R)
BARIUM SULFATE (UNII: 25BB7EKE2E)
PANTOTHENIC ACID (UNII: 19F5HK2737)
ASCORBIC ACID (UNII: PQ6CK8PD0R)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
VITAMIN A PALMITATE (UNII: 1D1K0N0VVC)
SQUALANE (UNII: GW89575KF9)
LEVOMENOL (UNII: 24WE03BX2T)
GLYCYRRHIZINATE DIPOTASSIUM (UNII: CA2Y0FE3FX)
POLYSORBATE 60 (UNII: CAL22UVI4M)
PEG-12 DIMETHICONE (300 CST) (UNII: ZEL54N6W95)
POLY(METHYL METHACRYLATE; 450000 MW) (UNII: Z47NNT4J11)
POLYSORBATE 20 (UNII: 7T1F30V5YH)
MAGNESIUM ALUMINUM SILICATE (UNII: 6M3P64V0NC)
EDETATE SODIUM (UNII: MP1J8420LU)
XANTHAN GUM (UNII: TTV12P4NEE)
HYDROXYETHYL ACRYLATE/SODIUM ACRYLOYLDIMETHYL TAURATE COPOLYMER (100000 MPA.S AT 1.5%) (UNII: 86FQE96TZ4)
CAPRYLYL GLYCOL (UNII: 00YIU5438U)
SORBIC ACID (UNII: X045WJ989B)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
FERRIC OXIDE RED (UNII: 1K09F3G675)
MICA (UNII: V8A1AW0880)
WATER (UNII: 059QF0KO0R)
PHENYL TRIMETHICONE (UNII: DR0K5NOJ4R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 69968-0115-1	32 mL in 1 TUBE; Type 0: Not a Combination Product	05/23/2013	11/30/2024

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M020	05/23/2013	11/30/2024

NEUTROGENA HEALTHY SKIN GLOW SHEERS ILLUMINATING TINTED MOISTURIZER - LIGHT TO MEDIUM 30  SUNSCREEN BROAD SPECTRUM SPF30
homosalate, octinoxate, octisalate, oxybenzone, and titanium dioxide liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 69968-0114
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
HOMOSALATE (UNII: V06SV4M95S) (HOMOSALATE - UNII:V06SV4M95S)	HOMOSALATE	50 mg  in 1 mL
OCTINOXATE (UNII: 4Y5P7MUD51) (OCTINOXATE - UNII:4Y5P7MUD51)	OCTINOXATE	75 mg  in 1 mL
OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W)	OCTISALATE	50 mg  in 1 mL
OXYBENZONE (UNII: 95OOS7VE0Y) (OXYBENZONE - UNII:95OOS7VE0Y)	OXYBENZONE	20 mg  in 1 mL
TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (TITANIUM DIOXIDE - UNII:15FIX9V2JP)	TITANIUM DIOXIDE	29 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
PHENYL TRIMETHICONE (UNII: DR0K5NOJ4R)
BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
PEG-100 STEARATE (UNII: YD01N1999R)
BARIUM SULFATE (UNII: 25BB7EKE2E)
PANTOTHENIC ACID (UNII: 19F5HK2737)
ASCORBIC ACID (UNII: PQ6CK8PD0R)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
VITAMIN A PALMITATE (UNII: 1D1K0N0VVC)
SQUALANE (UNII: GW89575KF9)
LEVOMENOL (UNII: 24WE03BX2T)
GLYCYRRHIZINATE DIPOTASSIUM (UNII: CA2Y0FE3FX)
POLYSORBATE 60 (UNII: CAL22UVI4M)
PEG-12 DIMETHICONE (300 CST) (UNII: ZEL54N6W95)
POLY(METHYL METHACRYLATE; 450000 MW) (UNII: Z47NNT4J11)
POLYSORBATE 20 (UNII: 7T1F30V5YH)
MAGNESIUM ALUMINUM SILICATE (UNII: 6M3P64V0NC)
EDETATE SODIUM (UNII: MP1J8420LU)
XANTHAN GUM (UNII: TTV12P4NEE)
HYDROXYETHYL ACRYLATE/SODIUM ACRYLOYLDIMETHYL TAURATE COPOLYMER (100000 MPA.S AT 1.5%) (UNII: 86FQE96TZ4)
CAPRYLYL GLYCOL (UNII: 00YIU5438U)
SORBIC ACID (UNII: X045WJ989B)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
FERRIC OXIDE RED (UNII: 1K09F3G675)
MICA (UNII: V8A1AW0880)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 69968-0114-1	32 mL in 1 TUBE; Type 0: Not a Combination Product	05/23/2013	12/31/2024

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M020	05/23/2013	12/31/2024

Labeler - Johnson & Johnson Consumer Inc. (118772437)