Label: PENTOXIFYLLINE 0.5% / TRIAMCINOLONE ACETONIDE 0.1% gel
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Contains inactivated NDC Code(s)
NDC Code(s): 72934-1169-2 - Packager: Sincerus Florida, LLC
- Category: HUMAN PRESCRIPTION DRUG LABEL
- DEA Schedule: None
- Marketing Status: unapproved drug other
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Drug Label Information
Updated May 14, 2019
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- Official Label (Printer Friendly)
- Directions for use
- Sincerus Florida, LLC. Adverse reactions
- Active, inactive
- NDC 72934- 1169-2 PENTOXIFYLLINE USP 0.5% / TRIAMCINOLONE ACETONIDE USP 0.1%. Gel 30gm.
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INGREDIENTS AND APPEARANCE
PENTOXIFYLLINE 0.5% / TRIAMCINOLONE ACETONIDE 0.1%
pentoxifylline 0.5% / triamcinolone acetonide 0.1% gelProduct Information Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:72934-1169 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength PENTOXIFYLLINE (UNII: SD6QCT3TSU) (PENTOXIFYLLINE - UNII:SD6QCT3TSU) PENTOXIFYLLINE 0.5 g in 100 g TRIAMCINOLONE ACETONIDE (UNII: F446C597KA) (TRIAMCINOLONE ACETONIDE - UNII:F446C597KA) TRIAMCINOLONE ACETONIDE 0.1 g in 100 g Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:72934-1169-2 30 g in 1 BOTTLE, PUMP; Type 0: Not a Combination Product 05/15/2019 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 05/15/2019 Labeler - Sincerus Florida, LLC (080105003) Establishment Name Address ID/FEI Business Operations Sincerus Florida, LLC 080105003 manufacture(72934-1169)
