Medication Guide App

La RochePosay Laboratoire Dermatologique Anthelios 50 Mineral Ultra Light Sunscreen

Dosage form: lotion
Ingredients: Titanium dioxide 5.5mL in 50mL
Labeler: L'Oreal USA Products Inc
NDC Code: 49967-090

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

Drug Facts

Active ingredientsTitanium dioxide 11%

Warnings

For external use only

When using this product keep out of eyes. Rinse with water to remove.

Stop use and consult a doctor if rash or irritation develops and lasts

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Directionsshake well before use
apply evenly before sun exposure
reapply as needed or after towel drying, swimming, or perspiring
children under 6 months of age: ask a doctor

Inactive ingredientswater, isododecane, C12-15 alkyl benzoate, dimethicone, undecane, triethylhexanoin, isohexadecane, styrene/acrylates copolymer, nylon-12, caprylyl methicone, butyloctyl salicylate, phenethyl benzoate, silica, tridecane, dicaprylyl carbonate, dicaprylyl ether, talc, dimethicone/PEG-10/15 crosspolymer, aluminum stearate, pentylene glycol, PEG-9 polydimethylsiloxyethyl dimethicone, alumina, polyhydroxystearic acid, phenoxyethanol, magnesium sulfate, protpylene glycol, caprylyl glycol, aluminum hydroxide, PEG-8 laurate, stearic acid, disteardimonium hectorite, diethylhexyl syringylidenemalonate, tocopherol, propylene carbonate, cassia alata leaf extract, maltodextrin, benzoic acid, PEG-9

Uses

helps prevent sunburn

higher SPF gives more sunburn protection

retains SPF after 40 minutes of activity in the water or perspiring


LA ROCHEPOSAY LABORATOIRE DERMATOLOGIQUE  ANTHELIOS 50 MINERAL ULTRA LIGHT SUNSCREEN
titanium dioxide lotion
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:49967-090
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
Titanium dioxide (Titanium dioxide) Titanium dioxide5.5 mL  in 50 mL
Packaging
#Item CodePackage Description
1NDC:49967-090-011 BOTTLE, PLASTIC (BOTTLE) in 1 CARTON
150 mL in 1 BOTTLE, PLASTIC
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart35207/01/2011
Labeler - L'Oreal USA Products Inc (002136794)
Establishment
NameAddressID/FEIOperations
Goodier Cosmetics LP007317209manufacture

Revised: 12/2011
 
L'Oreal USA Products Inc

Disclaimer: Every effort has been made to ensure that the information provided here is accurate, up-to-date and complete, but no guarantee is made to that effect. Drug information contained herein may be time sensitive. This information has been compiled for use by healthcare practitioners and consumers in the United States. The absence of a warning for a given drug or combination thereof in no way should be construed to indicate that the drug or combination is safe, effective or appropriate for any given patient. If you have questions about the substances you are taking, check with your doctor, nurse or pharmacist.

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