Label: NEUTROGENA HEALTHY SKIN RADIANT TINTED MOISTURIZER SUNSCREEN BROAD SPECTRUM SPF 30, SHEER IVORY 10- homosalate, octinoxate, octisalate, oxybenzone, and titanium dioxide lotion
NEUTROGENA HEALTHY SKIN RADIANT TINTED MOISTURIZER SUNSCREEN BROAD SPECTRUM SPF 30, SHEER FAIR 20- homosalate, octinoxate, octisalate, oxybenzone, and titanium dioxide lotion
NEUTROGENA HEALTHY SKIN RADIANT TINTED MOISTURIZER SUNSCREEN BROAD SPECTRUM SPF 30, SHEER TAN 30- homosalate, octinoxate, octisalate, oxybenzone, and titanium dioxide lotion
- NDC Code(s): 69968-0607-1, 69968-0608-1, 69968-0609-1
- Packager: Johnson & Johnson Consumer Inc.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated April 19, 2024
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- SPL UNCLASSIFIED SECTION
- ACTIVE INGREDIENT
-
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
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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
-
Inactive ingredients
Water, Phenyl Trimethicone, Cetyl Dimethicone, Butylene Glycol, Silica, Cetearyl Alcohol, Barium Sulfate, PEG-100 Stearate, Glyceryl Stearate, Hydroxyethyl Acrylate/Sodium Acryloyldimethyl Taurate Copolymer, Phenoxyethanol, Squalane, Bisabolol, Caprylyl Glycol, Magnesium Aluminum Silicate, Dipotassium Glycyrrhizate, Polysorbate 20, Polymethyl Methacrylate, Cetyl Hydroxyethylcellulose, Polysorbate 60, Xanthan Gum, Tetrasodium EDTA, Sorbic Acid, PEG-12 Dimethicone, Tocopheryl Acetate, Pantothenic Acid, Retinyl Palmitate, Ascorbic Acid, Iron Oxides, Mica, Titanium Dioxide
- Questions?
- SPL UNCLASSIFIED SECTION
- PRINCIPAL DISPLAY PANEL - 32 mL Tube Label - sheer ivory 10
- PRINCIPAL DISPLAY PANEL - 32 mL Tube Label - sheer fair 20
- PRINCIPAL DISPLAY PANEL - 32 mL Tube Label - sheer tan 30
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INGREDIENTS AND APPEARANCE
NEUTROGENA HEALTHY SKIN RADIANT TINTED MOISTURIZER SUNSCREEN BROAD SPECTRUM SPF 30, SHEER IVORY 10
homosalate, octinoxate, octisalate, oxybenzone, and titanium dioxide lotionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:69968-0607 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) CETYL DIMETHICONE 25 (UNII: U4AS1BW4ZB) BUTYLENE GLYCOL (UNII: 3XUS85K0RA) SILICON DIOXIDE (UNII: ETJ7Z6XBU4) CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S) BARIUM SULFATE (UNII: 25BB7EKE2E) PEG-100 STEARATE (UNII: YD01N1999R) GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4) HYDROXYETHYL ACRYLATE/SODIUM ACRYLOYLDIMETHYL TAURATE COPOLYMER (100000 MPA.S AT 1.5%) (UNII: 86FQE96TZ4) PHENOXYETHANOL (UNII: HIE492ZZ3T) SQUALANE (UNII: GW89575KF9) LEVOMENOL (UNII: 24WE03BX2T) CAPRYLYL GLYCOL (UNII: 00YIU5438U) MAGNESIUM ALUMINUM SILICATE (UNII: 6M3P64V0NC) GLYCYRRHIZINATE DIPOTASSIUM (UNII: CA2Y0FE3FX) POLYSORBATE 20 (UNII: 7T1F30V5YH) POLY(METHYL METHACRYLATE; 450000 MW) (UNII: Z47NNT4J11) CETYL HYDROXYETHYLCELLULOSE (350000 MW) (UNII: T7SWE4S2TT) POLYSORBATE 60 (UNII: CAL22UVI4M) XANTHAN GUM (UNII: TTV12P4NEE) EDETATE SODIUM (UNII: MP1J8420LU) SORBIC ACID (UNII: X045WJ989B) VITAMIN A PALMITATE (UNII: 1D1K0N0VVC) PEG-12 DIMETHICONE (300 CST) (UNII: ZEL54N6W95) .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) PANTOTHENIC ACID (UNII: 19F5HK2737) ASCORBIC ACID (UNII: PQ6CK8PD0R) FERRIC OXIDE RED (UNII: 1K09F3G675) MICA (UNII: V8A1AW0880) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:69968-0607-1 32 mL in 1 TUBE; Type 0: Not a Combination Product 11/04/2019 05/31/2025 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M020 11/04/2019 05/31/2025 NEUTROGENA HEALTHY SKIN RADIANT TINTED MOISTURIZER SUNSCREEN BROAD SPECTRUM SPF 30, SHEER FAIR 20
homosalate, octinoxate, octisalate, oxybenzone, and titanium dioxide lotionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:69968-0608 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) CETYL DIMETHICONE 25 (UNII: U4AS1BW4ZB) BUTYLENE GLYCOL (UNII: 3XUS85K0RA) SILICON DIOXIDE (UNII: ETJ7Z6XBU4) CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S) BARIUM SULFATE (UNII: 25BB7EKE2E) PEG-100 STEARATE (UNII: YD01N1999R) GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4) HYDROXYETHYL ACRYLATE/SODIUM ACRYLOYLDIMETHYL TAURATE COPOLYMER (100000 MPA.S AT 1.5%) (UNII: 86FQE96TZ4) PHENOXYETHANOL (UNII: HIE492ZZ3T) SQUALANE (UNII: GW89575KF9) LEVOMENOL (UNII: 24WE03BX2T) CAPRYLYL GLYCOL (UNII: 00YIU5438U) MAGNESIUM ALUMINUM SILICATE (UNII: 6M3P64V0NC) GLYCYRRHIZINATE DIPOTASSIUM (UNII: CA2Y0FE3FX) POLYSORBATE 20 (UNII: 7T1F30V5YH) POLY(METHYL METHACRYLATE; 450000 MW) (UNII: Z47NNT4J11) CETYL HYDROXYETHYLCELLULOSE (350000 MW) (UNII: T7SWE4S2TT) POLYSORBATE 60 (UNII: CAL22UVI4M) XANTHAN GUM (UNII: TTV12P4NEE) EDETATE SODIUM (UNII: MP1J8420LU) SORBIC ACID (UNII: X045WJ989B) PEG-12 DIMETHICONE (300 CST) (UNII: ZEL54N6W95) .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) PANTOTHENIC ACID (UNII: 19F5HK2737) VITAMIN A PALMITATE (UNII: 1D1K0N0VVC) ASCORBIC ACID (UNII: PQ6CK8PD0R) FERRIC OXIDE RED (UNII: 1K09F3G675) MICA (UNII: V8A1AW0880) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:69968-0608-1 32 mL in 1 TUBE; Type 0: Not a Combination Product 11/04/2019 01/31/2024 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M020 11/04/2019 01/31/2024 NEUTROGENA HEALTHY SKIN RADIANT TINTED MOISTURIZER SUNSCREEN BROAD SPECTRUM SPF 30, SHEER TAN 30
homosalate, octinoxate, octisalate, oxybenzone, and titanium dioxide lotionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:69968-0609 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 GLYCYRRHIZINATE DIPOTASSIUM (UNII: CA2Y0FE3FX) POLYSORBATE 20 (UNII: 7T1F30V5YH) POLY(METHYL METHACRYLATE; 450000 MW) (UNII: Z47NNT4J11) CETYL HYDROXYETHYLCELLULOSE (350000 MW) (UNII: T7SWE4S2TT) POLYSORBATE 60 (UNII: CAL22UVI4M) XANTHAN GUM (UNII: TTV12P4NEE) EDETATE SODIUM (UNII: MP1J8420LU) SORBIC ACID (UNII: X045WJ989B) PEG-12 DIMETHICONE (300 CST) (UNII: ZEL54N6W95) .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) PANTOTHENIC ACID (UNII: 19F5HK2737) VITAMIN A PALMITATE (UNII: 1D1K0N0VVC) ASCORBIC ACID (UNII: PQ6CK8PD0R) FERRIC OXIDE RED (UNII: 1K09F3G675) MICA (UNII: V8A1AW0880) PHENYL TRIMETHICONE (UNII: DR0K5NOJ4R) CETYL DIMETHICONE 25 (UNII: U4AS1BW4ZB) BUTYLENE GLYCOL (UNII: 3XUS85K0RA) SILICON DIOXIDE (UNII: ETJ7Z6XBU4) CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S) BARIUM SULFATE (UNII: 25BB7EKE2E) PEG-100 STEARATE (UNII: YD01N1999R) GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4) HYDROXYETHYL ACRYLATE/SODIUM ACRYLOYLDIMETHYL TAURATE COPOLYMER (100000 MPA.S AT 1.5%) (UNII: 86FQE96TZ4) PHENOXYETHANOL (UNII: HIE492ZZ3T) SQUALANE (UNII: GW89575KF9) LEVOMENOL (UNII: 24WE03BX2T) CAPRYLYL GLYCOL (UNII: 00YIU5438U) MAGNESIUM ALUMINUM SILICATE (UNII: 6M3P64V0NC) WATER (UNII: 059QF0KO0R) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:69968-0609-1 32 mL in 1 TUBE; Type 0: Not a Combination Product 11/04/2019 05/31/2025 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M020 11/04/2019 05/31/2025 Labeler - Johnson & Johnson Consumer Inc. (118772437)
