Label: DESOXIMETASONE 0.05% / HYDROQUINONE 6% / TRETINOIN 0.05% emulsion
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Contains inactivated NDC Code(s)
NDC Code(s): 72934-6067-2 - Packager: Sincerus Florida, LLC
- Category: HUMAN PRESCRIPTION DRUG LABEL
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Drug Label Information
Updated May 20, 2019
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- Official Label (Printer Friendly)
- Directions for use
- Sincerus Florida, LLC. Adverse reaction
- Active, inactive
- NDC 72934- 6067-2 DESOXIMETASONE USP 0.05% / HYDROQUINONE USP 6% / TRETINOIN USP 0.05%. Emulsion 30 gm
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INGREDIENTS AND APPEARANCE
DESOXIMETASONE 0.05% / HYDROQUINONE 6% / TRETINOIN 0.05%
desoximetasone 0.05% / hydroquinone 6% / tretinoin 0.05% emulsionProduct Information Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:72934-6067 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength DESOXIMETASONE (UNII: 4E07GXB7AU) (DESOXIMETASONE - UNII:4E07GXB7AU) DESOXIMETASONE 0.05 g in 100 g HYDROQUINONE (UNII: XV74C1N1AE) (HYDROQUINONE - UNII:XV74C1N1AE) HYDROQUINONE 6 g in 100 g TRETINOIN (UNII: 5688UTC01R) (TRETINOIN - UNII:5688UTC01R) TRETINOIN 0.05 g in 100 g Product Characteristics Color yellow Score Shape Size Flavor Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:72934-6067-2 30 g in 1 BOTTLE, PUMP; Type 0: Not a Combination Product 05/21/2019 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 05/21/2019 Labeler - Sincerus Florida, LLC (080105003) Establishment Name Address ID/FEI Business Operations Sincerus Florida, LLC 080105003 manufacture(72934-6067)
