BENZOCAINE 20% / LIDOCAINE 10% / TETRACAINE 10%

BENZOCAINE 20% / LIDOCAINE 10% / TETRACAINE 10%- lidocaine, benzocaine and tetracaine cream
Sincerus Florida, LLC

Disclaimer: This drug has not been found by FDA to be safe and effective, and this labeling has not been approved by FDA. For further information about unapproved drugs, click here.

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Sincerus Florida, LLC. Adverse reactions

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NDC 72934- 2179-4 BENZOCAINE USP 20% / LIDOCAINE USP 10% / TETRACAINE USP 10%. Cream 120gm

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BENZOCAINE 20% / LIDOCAINE 10% / TETRACAINE 10%
benzocaine 20% / lidocaine 10% / tetracaine 10% cream
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:72934-2179
Route of Administration TOPICAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
LIDOCAINE (LIDOCAINE) LIDOCAINE 10 g in 100 g
BENZOCAINE (BENZOCAINE) BENZOCAINE 20 g in 100 g
TETRACAINE (TETRACAINE) TETRACAINE 10 g in 100 g
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:72934-2179-4 120 g in 1 BOTTLE, PUMP None
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 Operations
Sincerus Florida, LLC 080105003 manufacture (72934-2179)

Revised: 05/2019 Sincerus Florida, LLC

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