Label: PRECAINE B CHOCOLATE MINT- benzocaine topical anesthetic gel
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Contains inactivated NDC Code(s)
NDC Code(s): 10866-0090-1 - Packager: Pascal Company, Inc.
- Category: HUMAN PRESCRIPTION DRUG LABEL
- DEA Schedule: None
- Marketing Status: unapproved drug other
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Drug Label Information
Updated January 22, 2020
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- Official Label (Printer Friendly)
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Directions:
Application Directions:
For topical use only
For best results apply to previously dried oral mucosa with cotton swab or similar applicator for adequate control of pain
Removal of excess saliva during application minimizes dilution of the anesthetic and permits maximum penetration
Not more than 1.2 mg per Kg body weight per patient should be applied during a 24 hour period
- Warnings
- Contraindications
- Other Information:
- Precaine B
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INGREDIENTS AND APPEARANCE
PRECAINE B CHOCOLATE MINT
benzocaine topical anesthetic gelProduct Information Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:10866-0090 Route of Administration DENTAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength BENZOCAINE (UNII: U3RSY48JW5) (BENZOCAINE - UNII:U3RSY48JW5) BENZOCAINE 221 mg in 1 g Product Characteristics Color green Score Shape Size Flavor CHOCOLATE, MINT Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:10866-0090-1 30 g in 1 JAR; Type 0: Not a Combination Product 08/16/2017 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 08/16/2017 Labeler - Pascal Company, Inc. (009260217) Establishment Name Address ID/FEI Business Operations Pascal Company, Inc. 009260217 manufacture(10866-0090)