Label: DERMA BLEMISH BALM BLEMISH BALM- adenosine cream
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Contains inactivated NDC Code(s)
NDC Code(s): 52554-4001-1 - 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 5, 2010
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- Official Label (Printer Friendly)
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ACTIVE INGREDIENT
Active Ingredients: Titanium dioxide, Arbutin, Adenosine
Uses
■ Helps relieve irritation, redness, blemished skin
■ Helps cover visible skin problem
■ Helps to repair aging skin including wrinkles
■ Helps prevent surnburn
■ Provides multi-function care of whitening
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
■ Don’t use on the part where there is injury, eczema, or dermatitis
Keep out of reach of the children
Direction
■ After following the daily skin routine, Apply the Derma Blemish Balm generously on face and sensitive area as the final step.
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
DERMA BLEMISH BALM BLEMISH BALM
adenosine creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:52554-4001 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ADENOSINE (UNII: K72T3FS567) (ADENOSINE - UNII:K72T3FS567) ADENOSINE 0.0004 mL in 1 mL TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (TITANIUM DIOXIDE - UNII:15FIX9V2JP) TITANIUM DIOXIDE 0.06 mL in 1 mL ARBUTIN (UNII: C5INA23HXF) (ARBUTIN - UNII:C5INA23HXF) ARBUTIN 0.02 mL in 1 mL Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:52554-4001-1 50 mL in 1 TUBE Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 08/05/2010 Labeler - Universal Cosmetic Co., Ltd (557795012)
