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Lancome Bienfait UV SPF 50 Plus Super Fluid Facial Sunscreen

Dosage form: lotion
Ingredients: Avobenzone 1.5mL in 50mL, Homosalate 7.5mL in 50mL, Octisalate 2.5mL in 50mL, Octocrylene 2.5mL in 50mL, Oxybenzone 3mL in 50mL
Labeler: L'Oreal USA Products Inc
NDC Code: 49967-542

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 ingredients

Avobenzone 3%

Homosalate 15%

Octisalate 5%

Octocrylene 5%

Oxybenzone 6%

Uses Directions

Uses

  • helps prevent sunburn
  • higher SPF gives more sunburn protection
  • retains SPF after 40 minutes of activity in the water or perspiring
  • provides protection from the UVA rays that may contribute to skin damage and premature aging of the skin
Directions
  • shake 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

Warnings

Warnings

For external use only

When using this product

  • keep out of eyes. Rinse with water to remove.

Stop use and ask 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.

Other information

Other information

store at 20-25o C (68-77oF)

Purpose

Purpose

Sunscreen

LANCOME BIENFAIT UV SPF 50 PLUS  SUPER FLUID FACIAL SUNSCREEN
avobenzone homosalate octisalate octocrylene oxybenzone lotion
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:49967-542
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
Avobenzone (Avobenzone) Avobenzone1.5 mL  in 50 mL
Homosalate (Homosalate) Homosalate7.5 mL  in 50 mL
Octisalate (Octisalate) Octisalate2.5 mL  in 50 mL
Octocrylene (Octocrylene) Octocrylene2.5 mL  in 50 mL
Oxybenzone (Oxybenzone) Oxybenzone3 mL  in 50 mL
Packaging
#Item CodePackage Description
1NDC:49967-542-011 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 finalpart35208/01/2010
Labeler - L'Oreal USA Products Inc (002136794)
Establishment
NameAddressID/FEIOperations
L'Oreal USA Products Inc185931458analysis
Establishment
NameAddressID/FEIOperations
Cosmetic Essence, LLC032565959manufacture

Revised: 07/2010
Document Id: 15b9ddb9-8c7c-428c-81cf-bc5bf40ea3e4
Set id: a7b1a954-62f8-4f4a-b1a2-34dbe429194e
Version: 1
Effective Time: 20100721
 
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 drug combination in no way should be construed to indicate that the drug or drug combination is safe, effective or appropriate for any given patient. If you have questions about the drugs you are taking, check with your doctor, nurse or pharmacist.

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