Label: FLUOCINONIDE 0.05% / HYALURONIC ACID SODIUM SALT 0.5% / NIACINAMIDE 4% cream
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Contains inactivated NDC Code(s)
NDC Code(s): 72934-2086-3 - Packager: Sincerus Florida, LLC
- Category: HUMAN PRESCRIPTION DRUG LABEL
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Drug Label Information
Updated May 22, 2019
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- Official Label (Printer Friendly)
- Directions for use
- Sincerus Florida, LLC. Adverse reactions
- Active, inactive
- NDC 72934- 2086-3 FLUOCINONIDE USP 0.05% / HYALURONIC ACID SODIUM SALT 0.5% / NIACINAMIDE USP 4%. Cream 60 gm.
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INGREDIENTS AND APPEARANCE
FLUOCINONIDE 0.05% / HYALURONIC ACID SODIUM SALT 0.5% / NIACINAMIDE 4%
fluocinonide 0.05% / hyaluronic acid sodium salt 0.5% / niacinamide 4% creamProduct Information Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:72934-2086 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength FLUOCINONIDE (UNII: 2W4A77YPAN) (FLUOCINONIDE - UNII:2W4A77YPAN) FLUOCINONIDE 0.05 g in 100 g HYALURONATE SODIUM (UNII: YSE9PPT4TH) (HYALURONIC ACID - UNII:S270N0TRQY) HYALURONATE SODIUM 0.5 g in 100 g Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:72934-2086-3 60 g in 1 BOTTLE, PUMP; Type 0: Not a Combination Product 05/22/2019 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 05/22/2019 Labeler - Sincerus Florida, LLC (080105003) Establishment Name Address ID/FEI Business Operations Sincerus Florida, LLC 080105003 manufacture(72934-2086)
