Label: LASER BLOCK 100 SUNBLOCK- octinoxate cream
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Contains inactivated NDC Code(s)
NDC Code(s): 52554-3001-1 - Packager: Universal Cosmetic Co., Ltd
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: unapproved drug other
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 Label Information
Updated August 4, 2010
If you are a consumer or patient please visit this version.
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- Official Label (Printer Friendly)
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ACTIVE INGREDIENT
Active ingredients: Ethylhexyl Methoxycinnamate, Zinc Oxide, 4-Methylbenzylidene camphor, Titanium Dioxide, Isoamyl p-Methoxycinnamate, Butyl MethoxydibenzoylmethaneUses
■ 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
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INGREDIENTS AND APPEARANCE
LASER BLOCK 100 SUNBLOCK
octinoxate creamProduct 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)
