Label: NEUTROGENA ULTRA SHEER FACE SUNSCREEN SPF 60- avobenzone, homosalate, octisalate, octocrylene stick
- NDC Code(s): 69968-0897-1
- Packager: Kenvue Brands LLC
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated November 12, 2024
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- 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
• 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
- 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, Styrene/Acrylates Copolymer, Tocopheryl Acetate, Ascorbyl Palmitate
- Questions or comments?
- SPL UNCLASSIFIED SECTION
- Neutrogena Ultra Sheer Face Stick Sunscreen SPF 60 - 13 g Canister in Blister Pack Label
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INGREDIENTS AND APPEARANCE
NEUTROGENA ULTRA SHEER FACE SUNSCREEN SPF 60
avobenzone, homosalate, octisalate, octocrylene stickProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:69968-0897 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength 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 HOMOSALATE (UNII: V06SV4M95S) (HOMOSALATE - UNII:V06SV4M95S) HOMOSALATE 150 mg in 1 g Inactive Ingredients Ingredient Name Strength BUTYLOCTYL SALICYLATE (UNII: 2EH13UN8D3) DIMETHICONE (UNII: 92RU3N3Y1O) ASCORBYL PALMITATE (UNII: QN83US2B0N) NEOPENTYL GLYCOL DIETHYLHEXANOATE (UNII: U68ZV6W62C) VINYLPYRROLIDONE/EICOSENE COPOLYMER (UNII: 035MV9S1C3) CERESIN (UNII: Q1LS2UJO3A) SYNTHETIC BEESWAX (UNII: 08MNR5YE2R) OCTYLDODECYL NEOPENTANOATE (UNII: X8725R883T) .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) PARAFFIN (UNII: I9O0E3H2ZE) NEOPENTYL GLYCOL DIISOSTEARATE (UNII: 4M6OQ34JWW) ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ) ISOHEXADECANE (UNII: 918X1OUF1E) DIETHYLHEXYL 2,6-NAPHTHALATE (UNII: I0DQJ7YGXM) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:69968-0897-1 1 in 1 BLISTER PACK 10/04/2024 1 13 g in 1 CANISTER; 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 10/04/2024 Labeler - Kenvue Brands LLC (118772437)
