Precaine Anesthetic Gel

Contains: Lidocaine 8%, Dibucaine 0.8%

in a flavored aqueous base.

Net Contents 30g

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 one ounce (28g) per patient should be applied during a 24 hour period.

Recommended dosage should not be exceeded due to possible side effects. Keep out of the reach of children. For professional use only. Do not use in the eyes. Avoid swallowing.

Precaine is contraindicated in patients with known hypersensitivity to amine or quinoline type anesthetics.

For product MSDS information please go to www.pascaldental.com or contact Pascal directly.

Precaine

Topical Anesthetic Gel for oral use

Strawberry

Precaine Label

PRECAINE
topical anesthetic gel gel

Product Information
Product Type	HUMAN PRESCRIPTION DRUG	Item Code (Source)	NDC:10866-0062
Route of Administration	BUCCAL, TOPICAL, DENTAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
LIDOCAINE (UNII: 98PI200987) (LIDOCAINE - UNII:98PI200987)	LIDOCAINE	80 mg in 1 g
DIBUCAINE (UNII: L6JW2TJG99) (DIBUCAINE - UNII:L6JW2TJG99)	DIBUCAINE	8 mg in 1 g

Product Characteristics
Color	red	Score
Shape		Size
Flavor	STRAWBERRY	Imprint Code
Contains

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:10866-0062-1	30 g in 1 JAR; Type 0: Not a Combination Product	08/01/2000

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
Export only		08/01/2000

Labeler - Pascal Company, Inc. (009260217)

Registrant - Alexia Petropoulos (009260217)

Name	Address	ID/FEI	Business Operations
Establishment
Pascal Company, Inc.		009260217	manufacture(10866-0062)