LASER BLOCK 100 SUNBLOCK- octinoxate cream

Laser Block 100 by

Drug Labeling and Warnings

Laser Block 100 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, Zinc Oxide,  4-Methylbenzylidene camphor, Titanium Dioxide, Isoamyl p-Methoxycinnamate, Butyl Methoxydibenzoylmethane

Uses
■ Perfectly blocks UV rays without stimuli
■ Effective against
l    PIH(Post Inflammatory Pigmentation)
l    Photosensitive skins
l    DNA destruction
■ Suitable for skin that underwent medical treatment
■ Helps keep moisturize


Warning
For external use only
When using this product
■    Avoid eye area. If contact occurs, rinse eyes thoroughly
■  If following abnormal symptoms occurs after use, stop use and ask doctor
l    red specks, swelling, itching
Keep out of reach of the children

    
Direction
■ Before finishing skincare, rub a proper quantity over the whole face that underwent IPL or Laser therapy.

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

LASER BLOCK 100  SUNBLOCK
octinoxate cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 52554-3001
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
OCTINOXATE (UNII: 4Y5P7MUD51) (OCTINOXATE - UNII:4Y5P7MUD51)	OCTINOXATE	0.07 mL  in 1 mL
ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z)	ZINC OXIDE	0.05 mL  in 1 mL
ENZACAMENE (UNII: 8I3XWY40L9) (ENZACAMENE - UNII:8I3XWY40L9)	ENZACAMENE	0.03 mL  in 1 mL
TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (TITANIUM DIOXIDE - UNII:15FIX9V2JP)	TITANIUM DIOXIDE	0.02 mL  in 1 mL
AMILOXATE (UNII: 376KTP06K8) (AMILOXATE - UNII:376KTP06K8)	AMILOXATE	0.02 mL  in 1 mL
AVOBENZONE (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX)	AVOBENZONE	0.005 mL  in 1 mL

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 52554-3001-1	50 mL in 1 TUBE

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved drug other		08/04/2010

Labeler - Universal Cosmetic Co., Ltd (557795012)