LASER BLOCK 100 SUNBLOCK- octinoxate cream 
Universal Cosmetic Co., Ltd

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.

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Drug Facts

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.

package label
LASER BLOCK 100  SUNBLOCK
octinoxate cream
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:52554-3001
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
OCTINOXATE (UNII: 4Y5P7MUD51) (OCTINOXATE - UNII:4Y5P7MUD51) OCTINOXATE0.07 mL  in 1 mL
ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z) ZINC OXIDE0.05 mL  in 1 mL
ENZACAMENE (UNII: 8I3XWY40L9) (ENZACAMENE - UNII:8I3XWY40L9) ENZACAMENE0.03 mL  in 1 mL
TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (TITANIUM DIOXIDE - UNII:15FIX9V2JP) TITANIUM DIOXIDE0.02 mL  in 1 mL
AMILOXATE (UNII: 376KTP06K8) (AMILOXATE - UNII:376KTP06K8) AMILOXATE0.02 mL  in 1 mL
AVOBENZONE (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX) AVOBENZONE0.005 mL  in 1 mL
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:52554-3001-150 mL in 1 TUBE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
unapproved drug other08/04/2010
Labeler - Universal Cosmetic Co., Ltd (557795012)

Revised: 8/2010
Document Id: eed3377a-26c2-4e93-95c4-7f10712d90be
Set id: b81b277d-de03-4130-812b-37ef5d54feb2
Version: 1
Effective Time: 20100804
 
Universal Cosmetic Co., Ltd