Label: 141030 HYDROQUINONE 8% emulsion
- Category: HUMAN PRESCRIPTION DRUG LABEL
- DEA Schedule: None
- Marketing Status: unapproved drug other
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Updated July 2, 2020
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- Directions for use
- Sincerus Florida, LLC adverse reactions
- Active, inactive
- NDC 72934-6229-2 141030 HYDROQUINONE 8% emulsion 30 gm
INGREDIENTS AND APPEARANCE
141030 HYDROQUINONE 8%
141030 hydroquinone 8% emulsion
Product Information Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:72934-6229 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength HYDROQUINONE (UNII: XV74C1N1AE) (HYDROQUINONE - UNII:XV74C1N1AE) HYDROQUINONE 8 g in 100 g Product Characteristics Color yellow (Beige) Score Shape Size Flavor Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:72934-6229-2 30 g in 1 BOTTLE, PUMP; Type 0: Not a Combination Product 07/02/2020 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 07/02/2020 Labeler - Sincerus Florida, LLC (080105003) Establishment Name Address ID/FEI Business Operations Sincerus Florida, LLC 080105003 manufacture(72934-6229)