MediSpa Sunblock sunblock

Dosage form: cream
Ingredients: ZINC OXIDE 0.05mL in 1mL, OCTINOXATE 0.07mL in 1mL, ENZACAMENE 0.03mL in 1mL, AVOBENZONE 0.005mL in 1mL
Labeler: Universal Cosmetic Co., Ltd
NDC Code: 52554-1001

Disclaimer: This drug has not been found by FDA to be safe and effective, and this labeling has not been approved by FDA. For further information about unapproved drugs, click here.

Drug Facts

Active Ingredients: Ethylhexyl Methoxycinnamate, Zinc Oxide, 4-Methylbenzylidene camphor, Butyl Mehoxydibenzoylmethane

Uses
■ Perfectly blocks both UVA and UVB rays without stimuli
■ Provides high protection from sunburn
■ Suitable for skin that underwent medical treatment

Warning
For external use only
When using this product
■    Avoid eye area. If contact occurs, rinse eyes thoroughly
■  Discontinue use if signs of irritation develops
Keep out of reach of the children

Direction
■ Rub a proper quantity over the whole face, before finishing skincare.

Other Information
■ store between 20-25 °C (68-77 °F)
■ avoid freezing and excessive heat above 40 °C (104 °F)
■ close cap after use.

Inactive Ingredient
■ Water ■ Cyclomethicone ■ Dimethicone/Vinyl Dimethicone Crosspolymer ■ C12-15 Alkyl Benzoate ■ Glycerin ■ Cetyl PEG/PPG-10/1 Dimethicone ■ Beeswax ■ Sodium Chloride ■ Sorbitan Sesquiolate ■ C20-40 acid ■ Methylparaben ■ Polyethylene ■ Brassica Campestris Sterols ■ Propylparaben ■ Disodium EDTA

MEDISPA SUNBLOCK  SUNBLOCK
zinc oxide cream
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:52554-1001
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ZINC OXIDE (ZINC OXIDE) ZINC OXIDE0.05 mL  in 1 mL
OCTINOXATE (OCTINOXATE) OCTINOXATE0.07 mL  in 1 mL
ENZACAMENE (ENZACAMENE) ENZACAMENE0.03 mL  in 1 mL
AVOBENZONE (AVOBENZONE) AVOBENZONE0.005 mL  in 1 mL
Packaging
#Item CodePackage Description
1NDC:52554-1001-170 mL in 1 BOTTLE, WITH APPLICATOR
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
unapproved drug other08/04/2010
Labeler - Universal Cosmetic Co., Ltd (557795012)

Revised: 08/2010
 
Universal Cosmetic 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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