Label: 141030 HYDROQUINONE 8% emulsion
-
Contains inactivated NDC Code(s)
NDC Code(s): 72934-6229-2 - Packager: Sincerus Florida, LLC
- Category: HUMAN PRESCRIPTION DRUG LABEL
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 July 2, 2020
If you are a healthcare professional or from the pharmaceutical industry please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- 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% emulsionProduct 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)
