Label: NEUTROGENA SPORT ACTIVE DEFENSE SPF 70- avobenzone, homosalate, octisalate, octocrylene spray
- NDC Code(s): 69968-0823-5
- 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 INGREDIENT
- Uses
- Warnings
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Directions
▪ spray liberally and spread evenly by hand 15 minutes before sun exposure
▪ hold container 4-6 inches from the skin to apply. Rub in.
▪ do not spray directly into face. Spray on hands and then apply to face. Rub in.
▪ do not apply in windy conditions.
▪ use in a well-ventilated area
▪ 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
- Questions?
- SPL UNCLASSIFIED SECTION
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PRINCIPAL DISPLAY PANEL - 141 g Can Label
NEW
Neutrogena®
DERMATOLOGIST RECOMMENDED BRAND
Sport
active defense
sunscreen
70
BROAD SPECTRUM SPF 70
skin barrier protection
helioplex®
broad spectrum uva●uvb
ANTIOXIDANTS
VITAMINS C & E
SWEAT + SUN + H2O DEFENSE
protects & refreshes
non-sticky ● quick-drying
water resistant (80 minutes)
NET WT 5.0 OZ (141 g)
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INGREDIENTS AND APPEARANCE
NEUTROGENA SPORT ACTIVE DEFENSE SPF 70
avobenzone, homosalate, octisalate, octocrylene sprayProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:69968-0823 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength AVOBENZONE (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX) AVOBENZONE 30 mg in 1 g HOMOSALATE (UNII: V06SV4M95S) (HOMOSALATE - UNII:V06SV4M95S) HOMOSALATE 150 mg in 1 g OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM) OCTOCRYLENE 100 mg in 1 g OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W) OCTISALATE 50 mg in 1 g Inactive Ingredients Ingredient Name Strength ALCOHOL (UNII: 3K9958V90M) BUTYLOCTYL SALICYLATE (UNII: 2EH13UN8D3) ACRYLATE/ISOBUTYL METHACRYLATE/N-TERT-OCTYLACRYLAMIDE COPOLYMER (75000 MW) (UNII: JU3XHR8VWK) NEOPENTYL GLYCOL DIHEPTANOATE (UNII: 5LKW3C543X) DIETHYLHEXYL 2,6-NAPHTHALATE (UNII: I0DQJ7YGXM) ASCORBYL PALMITATE (UNII: QN83US2B0N) .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) ISOBUTANE (UNII: BXR49TP611) DICAPRYLYL CARBONATE (UNII: 609A3V1SUA) POLYESTER-7 (UNII: 0841698D2F) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:69968-0823-5 141 g in 1 CAN; Type 0: Not a Combination Product 12/04/2023 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M020 12/04/2023 Labeler - Kenvue Brands LLC (118772437)