Kiehls Since 1851 CrossTerrain UV Skin Protector SPF 50 Water and Sweat Resistant Sunscreen

Dosage form: ointment
Ingredients: Avobenzone 1.2g in 40g, Homosalate 4g in 40g, Octisalate 2g in 40g, Octocrylene 3g in 40g, Oxybenzone 2g in 40g
Labeler: L'Oreal USA Products Inc
NDC Code: 49967-382

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

ACTIVE INGREDIENTS:

Avobenzone 3%

Homosalate 10%

Octisalate 5%

Octocrylene 7.5%

Oxybenzone 5%

Uses: Directions:
USES: Helps prevent sunburn. Higher SPF gives more sunburn protection. Retains SPF after 40 minutes of activity in the water or perspiring.

DIRECTIONS: Apply evenly before sun exposure and as needed. Children under 6 months of age, ask a doctor.

Warnings

WARNINGS: For external use only. 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.

KIEHLS SINCE 1851 CROSSTERRAIN UV SKIN PROTECTOR  SPF 50 WATER AND SWEAT RESISTANT SUNSCREEN
avobenzone homosalate octisalate octocrylene oxybenzone ointment
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:49967-382
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
Avobenzone (Avobenzone) Avobenzone1.2 g  in 40 g
Homosalate (Homosalate) Homosalate4 g  in 40 g
Octisalate (Octisalate) Octisalate2 g  in 40 g
Octocrylene (Octocrylene) Octocrylene3 g  in 40 g
Oxybenzone (Oxybenzone) Oxybenzone2 g  in 40 g
Packaging
#Item CodePackage Description
1NDC:49967-382-0140 g in 1 JAR
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart35206/01/2010
Labeler - L'Oreal USA Products Inc (002136794)
Establishment
NameAddressID/FEIOperations
L'Oreal USA Products Inc185931458manufacture

Revised: 06/2010
 
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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