Label: LANCOME PARIS UV EXPERT AQUAGEL DEFENSE 50 PLUS SUNSCREEN BROAD SPECTRUM SPF 50 PLUS PRIMER AND MOISTURIZER- avobenzone, homosalate, octisalate and octocrylene cream
- NDC Code(s): 49967-142-01, 49967-142-02, 49967-142-03, 49967-142-04
- Packager: L'Oreal USA Products Inc
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated December 24, 2023
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- Official Label (Printer Friendly)
- Active ingredients
- Purpose
- Uses
- Warnings
- Flammable until dry.
- Do not use
- When using this product
- Stop use and ask a doctor if
- Keep out of reach of children.
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Directions
For sunscreen use:
● apply generously 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
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Inactive ingredients
water, alcohol denat., styrene/acrylates copolymer, dimethicone, acrylates/dimethicone copolymer, tocopherol, dicaprylyl ether, sodium polyacrylate, sodium dodecylbenzenesulfonate, sodium benzoate, diethylhexyl syringylidenemalonate, phenoxyethanol, PEG-8 laurate, trisodium ethylenediamine disuccinate, menthyl lactate, pentylene glycol, mentha piperita (peppermint) extract, xanthan gum, propanediol, leontopodium alpinum flower/leaf extract, caprylyl glycol, caprylic/capric triglyceride, acrylates/c10-30 alkyl acrylate crosspolymer, moringa oleifera seed extract, rosa meichibon/delgramaue callus, disodium phosphate, citric acid, potassium sorbate, glycerin, fragrance
- Questions or comments?
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
LANCOME PARIS UV EXPERT AQUAGEL DEFENSE 50 PLUS SUNSCREEN BROAD SPECTRUM SPF 50 PLUS PRIMER AND MOISTURIZER
avobenzone, homosalate, octisalate and octocrylene creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:49967-142 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 mL homosalate (UNII: V06SV4M95S) (HOMOSALATE - UNII:V06SV4M95S) homosalate 150 mg in 1 mL OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W) OCTISALATE 50 mg in 1 mL OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM) OCTOCRYLENE 70 mg in 1 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) ALCOHOL (UNII: 3K9958V90M) STYRENE/ACRYLAMIDE COPOLYMER (500000 MW) (UNII: 5Z4DPO246A) DIMETHICONE (UNII: 92RU3N3Y1O) 2-ETHYLHEXYL ACRYLATE, METHACRYLATE, METHYL METHACRYLATE, OR BUTYL METHACRYLATE/HYDROXYPROPYL DIMETHICONE COPOLYMER (30000-300000 MW) (UNII: S7ZA3CCJ4M) TOCOPHEROL (UNII: R0ZB2556P8) DICAPRYLYL ETHER (UNII: 77JZM5516Z) SODIUM POLYACRYLATE (2500000 MW) (UNII: 05I15JNI2J) SODIUM DODECYLBENZENESULFONATE (UNII: 554127163Y) SODIUM BENZOATE (UNII: OJ245FE5EU) DIETHYLHEXYL SYRINGYLIDENEMALONATE (UNII: 3V5U97P248) PHENOXYETHANOL (UNII: HIE492ZZ3T) PEG-8 LAURATE (UNII: 762O8IWA10) TRISODIUM ETHYLENEDIAMINE DISUCCINATE (UNII: YA22H34H9Q) MENTHYL LACTATE, (-)- (UNII: 2BF9E65L7I) PENTYLENE GLYCOL (UNII: 50C1307PZG) MENTHA X PIPERITA WHOLE (UNII: 79M2M2UDA9) XANTHAN GUM (UNII: TTV12P4NEE) PROPANEDIOL (UNII: 5965N8W85T) LEONTOPODIUM NIVALE SUBSP. ALPINUM FLOWERING TOP (UNII: QQC1AK06RK) CAPRYLYL GLYCOL (UNII: 00YIU5438U) MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U) CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED) (UNII: 59TL3WG5CO) MORINGA OLEIFERA LEAF (UNII: 4WET1AWO9B) SODIUM PHOSPHATE, DIBASIC, ANHYDROUS (UNII: 22ADO53M6F) CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP) POTASSIUM SORBATE (UNII: 1VPU26JZZ4) GLYCERIN (UNII: PDC6A3C0OX) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:49967-142-01 1 in 1 CARTON 07/01/2021 1 30 mL in 1 TUBE; Type 0: Not a Combination Product 2 NDC:49967-142-02 1 in 1 CARTON 02/01/2022 2 10 mL in 1 TUBE; Type 0: Not a Combination Product 3 NDC:49967-142-03 1 in 1 CARTON 02/01/2022 12/30/2024 3 5 mL in 1 TUBE; Type 0: Not a Combination Product 4 NDC:49967-142-04 1 in 1 CARTON 02/01/2022 12/30/2024 4 1 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 M020 07/01/2021 Labeler - L'Oreal USA Products Inc (002136794) Establishment Name Address ID/FEI Business Operations SICOS ET CIE 276993581 manufacture(49967-142) , pack(49967-142)
