Label: BENZOCAINE 20% / LIDOCAINE 10% / TETRACAINE 10% cream
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Contains inactivated NDC Code(s)
NDC Code(s): 72934-2179-4 - 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 22, 2019
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- Official Label (Printer Friendly)
- Directions for use
- Sincerus Florida, LLC. Adverse reactions
- Active, inactive
- NDC 72934- 2179-4 BENZOCAINE USP 20% / LIDOCAINE USP 10% / TETRACAINE USP 10%. Cream 120gm
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INGREDIENTS AND APPEARANCE
BENZOCAINE 20% / LIDOCAINE 10% / TETRACAINE 10%
benzocaine 20% / lidocaine 10% / tetracaine 10% creamProduct Information Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:72934-2179 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength LIDOCAINE (UNII: 98PI200987) (LIDOCAINE - UNII:98PI200987) LIDOCAINE 10 g in 100 g BENZOCAINE (UNII: U3RSY48JW5) (BENZOCAINE - UNII:U3RSY48JW5) BENZOCAINE 20 g in 100 g TETRACAINE (UNII: 0619F35CGV) (TETRACAINE - UNII:0619F35CGV) TETRACAINE 10 g in 100 g Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:72934-2179-4 120 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(72934-2179)
