Label: HYALURONIC ACID SODIUM SALT 1% / HYDROQUINONE 6% emulsion
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Contains inactivated NDC Code(s)
NDC Code(s): 72934-6095-2 - 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 reactions
- Active, inactive
- NDC 72934- 6095-2 HYALURONIC ACID SODIUM SALT 1% / HYDROQUINONE USP 6%. Emulsion 30 gm.
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INGREDIENTS AND APPEARANCE
HYALURONIC ACID SODIUM SALT 1% / HYDROQUINONE 6%
hyaluronic acid sodium salt 1% / hydroquinone 6% emulsionProduct Information Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:72934-6095 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength HYDROQUINONE (UNII: XV74C1N1AE) (HYDROQUINONE - UNII:XV74C1N1AE) HYDROQUINONE 6 g in 100 g HYALURONATE SODIUM (UNII: YSE9PPT4TH) (HYALURONIC ACID - UNII:S270N0TRQY) HYALURONATE SODIUM 1 g in 100 g Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:72934-6095-2 30 g in 1 BOTTLE, PUMP; Type 0: Not a Combination Product 05/20/2019 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 05/20/2019 Labeler - Sincerus Florida, LLC (080105003) Establishment Name Address ID/FEI Business Operations Sincerus Florida, LLC 080105003 manufacture(72934-6095)
