LA ROCHE POSAY LABORATOIRE DERMATOLOGIQUE ANTHELIOS UV CORRECT BROAD SPECTRUM SPF 70 DAILY SUNSCREEN- avobenzone, homosalate, octisalate, and octocrylene lotion 
L'Oreal USA Products Inc

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Drug Facts

Active ingredients

Avobenzone 3%

Homosalate 13%

Octisalate 5%

Octocrylene 10%

Uses

Warnings

For external use only

Do not use

on damaged or broken skin

When using this product

keep out of eyes. Rinse with water to remove.

Stop use and ask a doctor if

rash occurs

Keep out of reach of children.

If swallowed, get medical help or contact a Poison Control Center right away.

Directions

For sunscreen use:

Purpose

Sunscreen

Other information

Inactive ingredients

water, polymethylsilsesquioxane, dimethicone, glycerin, dicaprylyl ether, niacinamide, poly c10-30 alkyl acrylate, styrene/acrylates copolymer, silica, caprylyl methicone, acrylates/dimethicone copolymer, diethylhexyl syringylidenemalonate, glyceryl stearate, PEG-100 stearate, phenoxyethanol, tocopherol, potassium cetyl phosphate, propylene glycol, caprylyl glycol, panthenol, acrylates/c10-30 alkyl acrylate crosspolymer, triethanolamine, PEG-8 laurate, inulin lauryl carbamate, chlorphenesin, trisodium ethylenediamine disuccinate, p-anisic acid, caprylic/capric triglyceride, xanthan gum, cassia alata leaf extract, maltodextrin, sodium dodecylbenzenesulfonate, disodium EDTA

Questions or comments?

1-888-LRP-LABO  1-888-577-5226

Monday - Friday (9 a.m. - 5 p.m. EST)

image of as carton

image of as carton
LA ROCHE POSAY LABORATOIRE DERMATOLOGIQUE ANTHELIOS UV CORRECT BROAD SPECTRUM SPF 70 DAILY SUNSCREEN 
avobenzone, homosalate, octisalate, and octocrylene lotion
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:49967-910
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
Avobenzone (UNII: G63QQF2NOX) (Avobenzone - UNII:G63QQF2NOX) Avobenzone30 mg  in 1 mL
Homosalate (UNII: V06SV4M95S) (Homosalate - UNII:V06SV4M95S) Homosalate130 mg  in 1 mL
Octisalate (UNII: 4X49Y0596W) (Octisalate - UNII:4X49Y0596W) Octisalate50 mg  in 1 mL
Octocrylene (UNII: 5A68WGF6WM) (Octocrylene - UNII:5A68WGF6WM) Octocrylene100 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
POLYMETHYLSILSESQUIOXANE (4.5 MICRONS) (UNII: 59Z907ZB69)  
DIMETHICONE (UNII: 92RU3N3Y1O)  
GLYCERIN (UNII: PDC6A3C0OX)  
DICAPRYLYL ETHER (UNII: 77JZM5516Z)  
NIACINAMIDE (UNII: 25X51I8RD4)  
BEHENYL ACRYLATE POLYMER (UNII: D64PM5UT4U)  
STYRENE/ACRYLAMIDE COPOLYMER (500000 MW) (UNII: 5Z4DPO246A)  
SILICON DIOXIDE (UNII: ETJ7Z6XBU4)  
CAPRYLYL TRISILOXANE (UNII: Q95M2P1KJL)  
2-ETHYLHEXYL ACRYLATE, METHACRYLATE, METHYL METHACRYLATE, OR BUTYL METHACRYLATE/HYDROXYPROPYL DIMETHICONE COPOLYMER (30000-300000 MW) (UNII: S7ZA3CCJ4M)  
DIETHYLHEXYL SYRINGYLIDENEMALONATE (UNII: 3V5U97P248)  
GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)  
PEG-100 STEARATE (UNII: YD01N1999R)  
PHENOXYETHANOL (UNII: HIE492ZZ3T)  
TOCOPHEROL (UNII: R0ZB2556P8)  
POTASSIUM CETYL PHOSPHATE (UNII: 03KCY6P7UT)  
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
CAPRYLYL GLYCOL (UNII: 00YIU5438U)  
PANTHENOL (UNII: WV9CM0O67Z)  
CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED) (UNII: 59TL3WG5CO)  
TROLAMINE (UNII: 9O3K93S3TK)  
PEG-8 LAURATE (UNII: 762O8IWA10)  
CHLORPHENESIN (UNII: I670DAL4SZ)  
TRISODIUM ETHYLENEDIAMINE DISUCCINATE (UNII: YA22H34H9Q)  
P-ANISIC ACID (UNII: 4SB6Y7DMM3)  
MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)  
XANTHAN GUM (UNII: TTV12P4NEE)  
SENNA ALATA LEAF (UNII: 4BXR6YZN92)  
MALTODEXTRIN (UNII: 7CVR7L4A2D)  
SODIUM DODECYLBENZENESULFONATE (UNII: 554127163Y)  
EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:49967-910-011 in 1 CARTON07/15/2021
150 mL in 1 BOTTLE; Type 0: Not a Combination Product
2NDC:49967-910-021 in 1 CARTON07/15/2021
25 mL in 1 TUBE; Type 0: Not a Combination Product
3NDC:49967-910-032 mL in 1 PACKET; Type 0: Not a Combination Product07/15/2021
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM02007/15/2021
Labeler - L'Oreal USA Products Inc (002136794)
Establishment
NameAddressID/FEIBusiness Operations
L'Oreal USA Products Inc185931458pack(49967-910) , manufacture(49967-910)

Revised: 12/2023
Document Id: 637ff496-97a6-4e1d-b73f-76cf42b70acc
Set id: a7c01228-02db-49a8-bb91-cee13fbd1df1
Version: 6
Effective Time: 20231231
 
L'Oreal USA Products Inc