Label: NEUTROGENA BEACH DEFENSE KIDS SUNSCREEN SPF 60 PLUS- avobenzone, homosalate, octisalate, octocrylene stick
- NDC Code(s): 69968-0816-2
- Packager: Johnson & Johnson Consumer Inc.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated October 20, 2023
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- Official Label (Printer Friendly)
- SPL UNCLASSIFIED SECTION
- Active ingredients
- Uses
- Warnings
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Directions
▪ apply liberally and evenly 15 minutes before sun exposure
▪ ensure complete coverage to the area above the lip, nose and tops of ears
▪ 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
▪ After use, twist stick down prior to capping to ensure complete closure.
- Other information
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Inactive ingredients
Neopentyl Glycol Diethylhexanoate, Octyldodecyl Neopentanoate, Synthetic Wax, Isohexadecane, Butyloctyl Salicylate, Ozokerite, Paraffin, Synthetic Beeswax, C12-15 Alkyl Benzoate, VP/Eicosene Copolymer, Neopentyl Glycol Diisostearate, Dimethicone, Diethylhexyl 2,6-Naphthalate, Tocopheryl Acetate, Ascorbyl Palmitate, Styrene/Acrylates Copolymer, Fragrance
- Questions?
- SPL UNCLASSIFIED SECTION
- PRINCIPAL DISPLAY PANEL - 42 g Canister
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INGREDIENTS AND APPEARANCE
NEUTROGENA BEACH DEFENSE KIDS SUNSCREEN SPF 60 PLUS
avobenzone, homosalate, octisalate, octocrylene stickProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:69968-0816 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength HOMOSALATE (UNII: V06SV4M95S) (HOMOSALATE - UNII:V06SV4M95S) HOMOSALATE 150 mg in 1 g OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W) OCTISALATE 50 mg in 1 g OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM) OCTOCRYLENE 100 mg in 1 g AVOBENZONE (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX) AVOBENZONE 30 mg in 1 g Inactive Ingredients Ingredient Name Strength OCTYLDODECYL NEOPENTANOATE (UNII: X8725R883T) ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ) DIMETHICONE (UNII: 92RU3N3Y1O) ISOHEXADECANE (UNII: 918X1OUF1E) CERESIN (UNII: Q1LS2UJO3A) PARAFFIN (UNII: I9O0E3H2ZE) DIETHYLHEXYL 2,6-NAPHTHALATE (UNII: I0DQJ7YGXM) SYNTHETIC BEESWAX (UNII: 08MNR5YE2R) NEOPENTYL GLYCOL DIISOSTEARATE (UNII: 4M6OQ34JWW) NEOPENTYL GLYCOL DIETHYLHEXANOATE (UNII: U68ZV6W62C) ALPHA-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) BUTYLOCTYL SALICYLATE (UNII: 2EH13UN8D3) ASCORBYL PALMITATE (UNII: QN83US2B0N) BUTYL METHACRYLATE/METHYL METHACRYLATE/METHACRYLIC ACID/STYRENE CROSSPOLYMER (UNII: V5RS026Q0H) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:69968-0816-2 42 g in 1 CANISTER; Type 0: Not a Combination Product 08/26/2023 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M020 08/26/2023 Labeler - Johnson & Johnson Consumer Inc. (118772437)
