Label: NEUTROGENA TRIPLE AGE REPAIR MOISTURIZER WITH SUNSCREEN BROAD SPECTRUM SPF 25- avobenzone, homosalate, octisalate, and octocrylene cream
- NDC Code(s): 69968-0414-1
- Packager: Johnson & Johnson Consumer Inc.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated October 16, 2023
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 INGREDIENT
-
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
-
Directions
For Sunscreen Use:
- apply liberally and evenly 15 minutes before sun exposure
- reapply at least every 2 hours
- use a water resistant sunscreen if swimming or sweating
-
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 ingredient
water, propylene glycol, glycerin, dimethicone, ethylhexyl palmitate, isononyl isononanoate, steareth-2, butyrospermum parkii (shea) butter, styrene/acrylates copolymer, methyl methacrylate crosspolymer, behenyl alcohol, hexylresorcinol, steareth-21, ammonium acryloyldimethyltaurate/VP copolymer, dimethicone crosspolymer, caprylyl glycol, phenoxyethanol, ascorbyl glucoside, fragrance, sclerotium gum, methylparaben, xylitylglucoside, ethylparaben, propylparaben, anhydroxylitol, disodium EDTA, sodium hydroxide, xylitol, bisabolol, mica, titanium dioxide
- Questions?
- SPL UNCLASSIFIED SECTION
- PRINCIPAL DISPLAY PANEL - 48 g Jar Carton
-
INGREDIENTS AND APPEARANCE
NEUTROGENA TRIPLE AGE REPAIR MOISTURIZER WITH SUNSCREEN BROAD SPECTRUM SPF 25
avobenzone, homosalate, octisalate, and octocrylene creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:69968-0414 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength AVOBENZONE (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX) AVOBENZONE 20 mg in 1 g HOMOSALATE (UNII: V06SV4M95S) (HOMOSALATE - UNII:V06SV4M95S) HOMOSALATE 40 mg in 1 g OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W) OCTISALATE 40 mg in 1 g OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM) OCTOCRYLENE 20 mg in 1 g Inactive Ingredients Ingredient Name Strength BUTYL METHACRYLATE/METHYL METHACRYLATE/METHACRYLIC ACID/STYRENE CROSSPOLYMER (UNII: V5RS026Q0H) WATER (UNII: 059QF0KO0R) PROPYLENE GLYCOL (UNII: 6DC9Q167V3) GLYCERIN (UNII: PDC6A3C0OX) DIMETHICONE (UNII: 92RU3N3Y1O) ETHYLHEXYL PALMITATE (UNII: 2865993309) ISONONYL ISONONANOATE (UNII: S4V5BS6GCX) STEARETH-2 (UNII: V56DFE46J5) SHEA BUTTER (UNII: K49155WL9Y) METHYL METHACRYLATE/GLYCOL DIMETHACRYLATE CROSSPOLYMER (UNII: 657L0NC5MT) DOCOSANOL (UNII: 9G1OE216XY) HEXYLRESORCINOL (UNII: R9QTB5E82N) STEARETH-21 (UNII: 53J3F32P58) AMMONIUM ACRYLOYLDIMETHYLTAURATE/VP COPOLYMER (UNII: W59H9296ZG) DIMETHICONE CROSSPOLYMER (450000 MPA.S AT 12% IN CYCLOPENTASILOXANE) (UNII: UF7620L1W6) CAPRYLYL GLYCOL (UNII: 00YIU5438U) PHENOXYETHANOL (UNII: HIE492ZZ3T) ASCORBYL GLUCOSIDE (UNII: 2V52R0NHXW) BETASIZOFIRAN (UNII: 2X51AD1X3T) METHYLPARABEN (UNII: A2I8C7HI9T) XYLITYLGLUCOSIDE (UNII: O0IEZ166FB) ETHYLPARABEN (UNII: 14255EXE39) PROPYLPARABEN (UNII: Z8IX2SC1OH) ANHYDROXYLITOL (UNII: 8XWR7NN42F) EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM) SODIUM HYDROXIDE (UNII: 55X04QC32I) XYLITOL (UNII: VCQ006KQ1E) LEVOMENOL (UNII: 24WE03BX2T) MICA (UNII: V8A1AW0880) TITANIUM DIOXIDE (UNII: 15FIX9V2JP) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:69968-0414-1 1 in 1 CARTON 10/30/2019 1 48 g in 1 JAR; 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 10/30/2019 Labeler - Johnson & Johnson Consumer Inc. (118772437)