Label: NDC 72934- 5010-4 BENZOCAINE 20% / LIDOCAINE 8% / TETRACAINE 4%. ointment
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Contains inactivated NDC Code(s)
NDC Code(s): 72934-5010-4 - Packager: Sincerus Florida, LLC
- Category: HUMAN PRESCRIPTION DRUG LABEL
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Drug Label Information
Updated May 17, 2019
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- Official Label (Printer Friendly)
- Directions for use
- Sincerus Florida, LLC. Adverse reactions
- Active, inactive
- NDC 72934- 5010-4 BENZOCAINE USP 20% / LIDOCAINE USP 8% / TETRACAINE USP 4%. Ointment 120gm
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INGREDIENTS AND APPEARANCE
NDC 72934- 5010-4 BENZOCAINE 20% / LIDOCAINE 8% / TETRACAINE 4%.
ndc 72934- 5010-4 benzocaine 20% / lidocaine 8% / tetracaine 4%. ointmentProduct Information Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:72934-5010 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength BENZOCAINE (UNII: U3RSY48JW5) (BENZOCAINE - UNII:U3RSY48JW5) BENZOCAINE 20 g in 100 g LIDOCAINE (UNII: 98PI200987) (LIDOCAINE - UNII:98PI200987) LIDOCAINE 8 g in 100 g TETRACAINE (UNII: 0619F35CGV) (TETRACAINE - UNII:0619F35CGV) TETRACAINE 4 g in 100 g Product Characteristics Color white Score Shape Size Flavor Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:72934-5010-4 120 g in 1 BOTTLE, PUMP; Type 0: Not a Combination Product 05/17/2019 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 05/17/2019 Labeler - Sincerus Florida, LLC (080105003) Establishment Name Address ID/FEI Business Operations Sincerus Florida, LLC 080105003 manufacture(72934-5010)
