Label: NEUTROGENA MINERAL UV TINT FACE MEDIUM DEEP SPF 30- titanium dioxide, zinc oxide lotion
NEUTROGENA MINERAL UV TINT FACE DEEP SPF 30- titanium dioxide, zinc oxide lotion
NEUTROGENA MINERAL UV TINT FACE LIGHT SPF 30- titanium dioxide, zinc oxide lotion
NEUTROGENA MINERAL UV TINT FACE MEDIUM SPF 30- titanium dioxide, zinc oxide lotion
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NDC Code(s):
69968-0781-1,
69968-0781-2,
69968-0782-1,
69968-0782-2, view more69968-0783-1, 69968-0783-2, 69968-0784-1, 69968-0784-2
- Packager: Kenvue Brands LLC
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated November 13, 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 ingredients
- Purpose
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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
- Shake well before use
- apply generously 15 minutes before sun exposure
- reapply:
- after 80 minutes of swimming or sweating
- immediately after towel drying
- at least every 2 hours
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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
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Inactive ingredients
Water, Isohexadecane, Dicaprylyl Carbonate, Dimethicone, Isopropyl Palmitate, Isononyl Isononanoate, Cetyl PEG/PPG-10/1 Dimethicone, C12-15 Alkyl Benzoate, Sodium Chloride, Polyhydroxystearic Acid, Tocopheryl Acetate, Triethoxycaprylylsilane, Sorbitan Sesquioleate, Phenoxyethanol, Ethylhexylglycerin, Dimethiconol, Aluminum Hydroxide, Dimethicone Crosspolymer, Stearic Acid, Xanthan Gum, Iron Oxides
- Questions?
- SPL UNCLASSIFIED SECTION
- PRINCIPAL DISPLAY PANEL - 32 mL Carton Label - LIGHT
- PRINCIPAL DISPLAY PANEL - 32 mL Carton Label - DEEP
- PRINCIPAL DISPLAY PANEL - 32 mL Carton Label - MEDIUM
- PRINCIPAL DISPLAY PANEL - 32 mL Carton Label - MEDIUM DEEP
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INGREDIENTS AND APPEARANCE
NEUTROGENA MINERAL UV TINT FACE MEDIUM DEEP SPF 30
titanium dioxide, zinc oxide lotionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:69968-0784 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z) ZINC OXIDE 216 mg in 1 mL TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (TITANIUM DIOXIDE - UNII:15FIX9V2JP) TITANIUM DIOXIDE 32 mg in 1 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) ISOHEXADECANE (UNII: 918X1OUF1E) DIMETHICONE (UNII: 92RU3N3Y1O) ISOPROPYL PALMITATE (UNII: 8CRQ2TH63M) CETYL PEG/PPG-10/1 DIMETHICONE (HLB 5) (UNII: 035JKJ76MT) ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ) SODIUM CHLORIDE (UNII: 451W47IQ8X) PHENOXYETHANOL (UNII: HIE492ZZ3T) ETHYLHEXYLGLYCERIN (UNII: 147D247K3P) ALUMINUM HYDROXIDE (UNII: 5QB0T2IUN0) XANTHAN GUM (UNII: TTV12P4NEE) FERRIC OXIDE RED (UNII: 1K09F3G675) STEARIC ACID (UNII: 4ELV7Z65AP) TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E) .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) DICAPRYLYL CARBONATE (UNII: 609A3V1SUA) ISONONYL ISONONANOATE (UNII: S4V5BS6GCX) SORBITAN SESQUIOLEATE (UNII: 0W8RRI5W5A) DIMETHICONE CROSSPOLYMER (450000 MPA.S AT 12% IN CYCLOPENTASILOXANE) (UNII: UF7620L1W6) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:69968-0784-1 1 in 1 CARTON 12/05/2022 1 32 mL in 1 TUBE; Type 0: Not a Combination Product 2 NDC:69968-0784-2 24 in 1 TRAY 03/04/2024 2 1.4 mL in 1 POUCH; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M020 12/05/2022 NEUTROGENA MINERAL UV TINT FACE DEEP SPF 30
titanium dioxide, zinc oxide lotionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:69968-0783 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z) ZINC OXIDE 216 mg in 1 mL TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (TITANIUM DIOXIDE - UNII:15FIX9V2JP) TITANIUM DIOXIDE 32 mg in 1 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) ISOHEXADECANE (UNII: 918X1OUF1E) DIMETHICONE (UNII: 92RU3N3Y1O) ISOPROPYL PALMITATE (UNII: 8CRQ2TH63M) CETYL PEG/PPG-10/1 DIMETHICONE (HLB 5) (UNII: 035JKJ76MT) ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ) SODIUM CHLORIDE (UNII: 451W47IQ8X) PHENOXYETHANOL (UNII: HIE492ZZ3T) ETHYLHEXYLGLYCERIN (UNII: 147D247K3P) ALUMINUM HYDROXIDE (UNII: 5QB0T2IUN0) XANTHAN GUM (UNII: TTV12P4NEE) FERRIC OXIDE RED (UNII: 1K09F3G675) STEARIC ACID (UNII: 4ELV7Z65AP) TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E) .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) DICAPRYLYL CARBONATE (UNII: 609A3V1SUA) ISONONYL ISONONANOATE (UNII: S4V5BS6GCX) SORBITAN SESQUIOLEATE (UNII: 0W8RRI5W5A) DIMETHICONE CROSSPOLYMER (450000 MPA.S AT 12% IN CYCLOPENTASILOXANE) (UNII: UF7620L1W6) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:69968-0783-1 1 in 1 CARTON 12/05/2022 1 32 mL in 1 TUBE; Type 0: Not a Combination Product 2 NDC:69968-0783-2 24 in 1 TRAY 03/04/2024 2 1.4 mL in 1 POUCH; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M020 12/05/2022 NEUTROGENA MINERAL UV TINT FACE LIGHT SPF 30
titanium dioxide, zinc oxide lotionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:69968-0781 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (TITANIUM DIOXIDE - UNII:15FIX9V2JP) TITANIUM DIOXIDE 32 mg in 1 mL ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z) ZINC OXIDE 216 mg in 1 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) ISOHEXADECANE (UNII: 918X1OUF1E) DIMETHICONE (UNII: 92RU3N3Y1O) ISOPROPYL PALMITATE (UNII: 8CRQ2TH63M) CETYL PEG/PPG-10/1 DIMETHICONE (HLB 5) (UNII: 035JKJ76MT) ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ) SODIUM CHLORIDE (UNII: 451W47IQ8X) PHENOXYETHANOL (UNII: HIE492ZZ3T) ETHYLHEXYLGLYCERIN (UNII: 147D247K3P) ALUMINUM HYDROXIDE (UNII: 5QB0T2IUN0) XANTHAN GUM (UNII: TTV12P4NEE) FERRIC OXIDE RED (UNII: 1K09F3G675) STEARIC ACID (UNII: 4ELV7Z65AP) TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E) .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) DICAPRYLYL CARBONATE (UNII: 609A3V1SUA) ISONONYL ISONONANOATE (UNII: S4V5BS6GCX) SORBITAN SESQUIOLEATE (UNII: 0W8RRI5W5A) DIMETHICONE CROSSPOLYMER (450000 MPA.S AT 12% IN CYCLOPENTASILOXANE) (UNII: UF7620L1W6) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:69968-0781-1 1 in 1 CARTON 12/05/2022 1 32 mL in 1 TUBE; Type 0: Not a Combination Product 2 NDC:69968-0781-2 24 in 1 TRAY 03/04/2024 2 1.4 mL in 1 POUCH; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M020 12/05/2022 NEUTROGENA MINERAL UV TINT FACE MEDIUM SPF 30
titanium dioxide, zinc oxide lotionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:69968-0782 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z) ZINC OXIDE 216 mg in 1 mL TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (TITANIUM DIOXIDE - UNII:15FIX9V2JP) TITANIUM DIOXIDE 32 mg in 1 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) ISOHEXADECANE (UNII: 918X1OUF1E) DIMETHICONE (UNII: 92RU3N3Y1O) ISOPROPYL PALMITATE (UNII: 8CRQ2TH63M) CETYL PEG/PPG-10/1 DIMETHICONE (HLB 5) (UNII: 035JKJ76MT) ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ) SODIUM CHLORIDE (UNII: 451W47IQ8X) PHENOXYETHANOL (UNII: HIE492ZZ3T) ETHYLHEXYLGLYCERIN (UNII: 147D247K3P) ALUMINUM HYDROXIDE (UNII: 5QB0T2IUN0) XANTHAN GUM (UNII: TTV12P4NEE) FERRIC OXIDE RED (UNII: 1K09F3G675) STEARIC ACID (UNII: 4ELV7Z65AP) TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E) .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) DICAPRYLYL CARBONATE (UNII: 609A3V1SUA) ISONONYL ISONONANOATE (UNII: S4V5BS6GCX) SORBITAN SESQUIOLEATE (UNII: 0W8RRI5W5A) DIMETHICONE CROSSPOLYMER (450000 MPA.S AT 12% IN CYCLOPENTASILOXANE) (UNII: UF7620L1W6) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:69968-0782-1 1 in 1 CARTON 12/05/2022 1 32 mL in 1 TUBE; Type 0: Not a Combination Product 2 NDC:69968-0782-2 24 in 1 TRAY 03/04/2024 2 1.4 mL in 1 POUCH; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M020 12/05/2022 Labeler - Kenvue Brands LLC (118772437)