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ATOMY SUN CREAM SPF 50 PA

Dosage form: cream
Ingredients: OCTINOXATE 4.5mL in 60mL, OCTISALATE 3mL in 60mL, ZINC OXIDE 2.9mL in 60mL, TITANIUM DIOXIDE 1.5mL in 60mL
Labeler: ATOMY CO LTD
NDC Code: 52257-1001

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.

ATOMY SUNCREAM SPF 50+PA+++

Drug Facts

Active ingredients
Octinoxate 7.5%
Octisalate 5.0%
Zinc Oxide 4.9%
Titanium Dioxide 2.49%

Uses
Helps prevent sunburn. Provides High protect from sunburn. Highter SPF gives more sunburn protection.

Directions
Apply after basic skin care product. Spread and appropriate amount entire face following the skin texture. Reapply as required.

Warnings
For external use only.
UV exposure from the sun increases the risk of skin cancer, premature skin aging, and other skin damage. It is important to decrease UV exposure by limiting time in the sun, wearing protective clothing, and using a sunscreen.
When using the product Keep out of eyes. Rinse with water to remove.
Keep out of reach of children if swallowed, get medical help or contact a Poison Control Center

ATOMY SUNCREAM SPF 50+PA+++

60ml/2fl.oz

ATOMY SUN CREAM SPF 50 PA 
octinoxate cream
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:52257-1001
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
OCTINOXATE (OCTINOXATE) OCTINOXATE4.5 mL  in 60 mL
OCTISALATE (OCTISALATE) OCTISALATE3 mL  in 60 mL
ZINC OXIDE (ZINC OXIDE) ZINC OXIDE2.9 mL  in 60 mL
TITANIUM DIOXIDE (TITANIUM DIOXIDE) TITANIUM DIOXIDE1.5 mL  in 60 mL
Product Characteristics
Coloryellow (yellow brown) Score    
ShapeSize
FlavorImprint Code
Contains    
Packaging
#Item CodePackage Description
1NDC:52257-1001-21 TUBE (TUBE) in 1 BOX
1NDC:52257-1001-160 mL in 1 TUBE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart35204/28/2010
Labeler - ATOMY CO LTD (631154601)

Revised: 04/2010
 
ATOMY CO LTD

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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