Label: NEUTROGENA ULTRA SHEER DRY TOUCH SUNSCREEN BROAD SPECTRUM SPF 55 CLUBTRAY- avobenzone, homosalate, octisalate, and octocrylene kit
- NDC Code(s): 69968-0576-3, 69968-0576-5, 69968-0847-9
- Packager: Johnson & Johnson Consumer Inc.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated December 6, 2023
If you are a consumer or patient please visit this version.
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- Official Label (Printer Friendly)
- Neutrogena® Ultra Sheer® dry-touch sunscreen BROAD SPECTRUM SPF55
- SPL UNCLASSIFIED SECTION
- ACTIVE INGREDIENT
- Uses
- Warnings
-
Directions
- apply liberally 15 minutes before sun exposure
- reapply:
- after 80 minutes of swimming or sweating
- immediately after towel drying
- at least every 2 hours
- 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, Styrene/Acrylates Copolymer, Silica, Dimethicone, Potassium Cetyl Phosphate, Benzyl Alcohol, Beeswax, Caprylyl Methicone, Glyceryl Stearate, PEG-100 Stearate, Cetyl Dimethicone, Caprylyl Glycol, Ethylhexylglycerin, Aluminum Starch Octenylsuccinate, Behenyl Alcohol, Acrylates/Dimethicone Copolymer, Xanthan Gum, Sodium Polyacrylate, Chlorphenesin, Dimethicone PEG - 10/15 Crosspolymer, Hydrolyzed Jojoba Esters, Fragrance, Disodium EDTA, Ethylhexyl Stearate, Tocopheryl Acetate, BHT, Trideceth-6, Jojoba Esters
- Questions?
- SPL UNCLASSIFIED SECTION
-
PRINCIPAL DISPLAY PANEL - Kit Package Label
Neutrogena®
#1 Dermatologist recommended suncare brand
Powerful sun protection,
unbelievably light feel
ACTUAL
SIZES
OXYBENZONE
& OCTINOXATE FREE
helioplex®
broad spectrum uva•uvb
NEUTROGENA® ULTRA SHEER® Sunscreen Lotion Broad Spectrum SPF 55
5.0 FL OZ (147 mL) and 3.0 FL OZ (88 mL), TOTAL 8.0 FL OZ (235 mL)
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INGREDIENTS AND APPEARANCE
NEUTROGENA ULTRA SHEER DRY TOUCH SUNSCREEN BROAD SPECTRUM SPF 55 CLUBTRAY
avobenzone, homosalate, octisalate, and octocrylene kitProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:69968-0847 Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:69968-0847-9 1 in 1 PACKAGE 12/08/2023 Quantity of Parts Part # Package Quantity Total Product Quantity Part 1 1 TUBE 147 mL Part 2 1 TUBE 88 mL Part 1 of 2 NEUTROGENA ULTRA SHEER DRY TOUCH SUNSCREEN BROAD SPECTRUM SPF55
avobenzone, homosalate, octisalate, and octocrylene lotionProduct Information Item Code (Source) NDC:69968-0576 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM) OCTOCRYLENE 100 mg in 1 mL HOMOSALATE (UNII: V06SV4M95S) (HOMOSALATE - UNII:V06SV4M95S) HOMOSALATE 100 mg in 1 mL AVOBENZONE (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX) AVOBENZONE 30 mg in 1 mL OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W) OCTISALATE 50 mg in 1 mL Inactive Ingredients Ingredient Name Strength XANTHAN GUM (UNII: TTV12P4NEE) EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM) CAPRYLYL GLYCOL (UNII: 00YIU5438U) JOJOBA OIL, RANDOMIZED (UNII: 7F0EV20QYL) SILICON DIOXIDE (UNII: ETJ7Z6XBU4) BENZYL ALCOHOL (UNII: LKG8494WBH) ALUMINUM STARCH OCTENYLSUCCINATE (UNII: I9PJ0O6294) DIMETHICONE/PEG-10/15 CROSSPOLYMER (UNII: 21AS8B1BSS) ETHYLHEXYL STEARATE (UNII: EG3PA2K3K5) CETYL DIMETHICONE 25 (UNII: U4AS1BW4ZB) PEG-100 STEARATE (UNII: YD01N1999R) TRIDECETH-6 (UNII: 3T5PCR2H0C) 2-ETHYLHEXYL ACRYLATE, METHACRYLATE, METHYL METHACRYLATE, OR BUTYL METHACRYLATE/HYDROXYPROPYL DIMETHICONE COPOLYMER (30000-300000 MW) (UNII: S7ZA3CCJ4M) DOCOSANOL (UNII: 9G1OE216XY) DIMETHICONE (UNII: 92RU3N3Y1O) YELLOW WAX (UNII: 2ZA36H0S2V) HYDROLYZED JOJOBA ESTERS (ACID FORM) (UNII: UDR641JW8W) GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4) ETHYLHEXYLGLYCERIN (UNII: 147D247K3P) CHLORPHENESIN (UNII: I670DAL4SZ) BUTYL METHACRYLATE/METHYL METHACRYLATE/METHACRYLIC ACID/STYRENE CROSSPOLYMER (UNII: V5RS026Q0H) BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K) WATER (UNII: 059QF0KO0R) POTASSIUM CETYL PHOSPHATE (UNII: 03KCY6P7UT) CAPRYLYL TRISILOXANE (UNII: Q95M2P1KJL) ALPHA-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:69968-0576-5 147 mL in 1 TUBE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M004 10/07/2019 Part 2 of 2 NEUTROGENA ULTRA SHEER DRY TOUCH SUNSCREEN BROAD SPECTRUM SPF55
avobenzone, homosalate, octisalate, and octocrylene lotionProduct Information Item Code (Source) NDC:69968-0576 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM) OCTOCRYLENE 100 mg in 1 mL HOMOSALATE (UNII: V06SV4M95S) (HOMOSALATE - UNII:V06SV4M95S) HOMOSALATE 100 mg in 1 mL OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W) OCTISALATE 50 mg in 1 mL AVOBENZONE (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX) AVOBENZONE 30 mg in 1 mL Inactive Ingredients Ingredient Name Strength 2-ETHYLHEXYL ACRYLATE, METHACRYLATE, METHYL METHACRYLATE, OR BUTYL METHACRYLATE/HYDROXYPROPYL DIMETHICONE COPOLYMER (30000-300000 MW) (UNII: S7ZA3CCJ4M) XANTHAN GUM (UNII: TTV12P4NEE) EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM) CAPRYLYL GLYCOL (UNII: 00YIU5438U) JOJOBA OIL, RANDOMIZED (UNII: 7F0EV20QYL) SILICON DIOXIDE (UNII: ETJ7Z6XBU4) BENZYL ALCOHOL (UNII: LKG8494WBH) ALUMINUM STARCH OCTENYLSUCCINATE (UNII: I9PJ0O6294) DIMETHICONE/PEG-10/15 CROSSPOLYMER (UNII: 21AS8B1BSS) ETHYLHEXYL STEARATE (UNII: EG3PA2K3K5) CETYL DIMETHICONE 25 (UNII: U4AS1BW4ZB) PEG-100 STEARATE (UNII: YD01N1999R) TRIDECETH-6 (UNII: 3T5PCR2H0C) DOCOSANOL (UNII: 9G1OE216XY) DIMETHICONE (UNII: 92RU3N3Y1O) YELLOW WAX (UNII: 2ZA36H0S2V) HYDROLYZED JOJOBA ESTERS (ACID FORM) (UNII: UDR641JW8W) GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4) ETHYLHEXYLGLYCERIN (UNII: 147D247K3P) CHLORPHENESIN (UNII: I670DAL4SZ) BUTYL METHACRYLATE/METHYL METHACRYLATE/METHACRYLIC ACID/STYRENE CROSSPOLYMER (UNII: V5RS026Q0H) BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K) WATER (UNII: 059QF0KO0R) POTASSIUM CETYL PHOSPHATE (UNII: 03KCY6P7UT) CAPRYLYL TRISILOXANE (UNII: Q95M2P1KJL) ALPHA-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:69968-0576-3 88 mL in 1 TUBE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M004 10/07/2019 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M020 12/08/2023 Labeler - Johnson & Johnson Consumer Inc. (118772437)