MEDISPA SUNSPRAY SUNBLOCK- octinoxate spray

MediSpa SunSpray by

Drug Labeling and Warnings

MediSpa SunSpray by is a Otc medication manufactured, distributed, or labeled by Universal Cosmetic Co., Ltd. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Active Ingredients: Ethylhexyl Methoxycinnamate, 4-Methylbenzylidene camphor, Octocrylene

 Uses
■ Helps prevent sunburn
■ Provides high protection from sunburn
■ Helps keep moisturize
■ Can be sprayed on powdered face

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
■ Spray 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.

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

MEDISPA SUNSPRAY  SUNBLOCK
octinoxate spray

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 52554-2001
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
OCTINOXATE (UNII: 4Y5P7MUD51) (OCTINOXATE - UNII:4Y5P7MUD51)	OCTINOXATE	0.075 mL  in 1 mL
ENZACAMENE (UNII: 8I3XWY40L9) (ENZACAMENE - UNII:8I3XWY40L9)	ENZACAMENE	0.05 mL  in 1 mL
OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM)	OCTOCRYLENE	0.01 mL  in 1 mL

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 52554-2001-1	55 mL in 1 BOTTLE, WITH APPLICATOR

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved drug other		08/06/2010

Labeler - Universal Cosmetic Co., Ltd (557795012)