Label: LIDOCAINE 2% / MUPIROCIN 2% ointment
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Contains inactivated NDC Code(s)
NDC Code(s): 72934-5139-2 - 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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- Sincerus Florida, LLC. Adverse reactions
- Active, inactive
- NDC 72934- 5139-2 LIDOCAINE 2% / MUPIROCIN 2%. Ointment 30gm.
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INGREDIENTS AND APPEARANCE
LIDOCAINE 2% / MUPIROCIN 2%
lidocaine 2% / mupirocin 2% ointmentProduct Information Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:72934-5139 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength MUPIROCIN (UNII: D0GX863OA5) (MUPIROCIN - UNII:D0GX863OA5) MUPIROCIN 2 g in 100 g LIDOCAINE (UNII: 98PI200987) (LIDOCAINE - UNII:98PI200987) LIDOCAINE 2 g in 100 g Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:72934-5139-2 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(72934-5139)
