Skip to Content

Gingicaine Gel Variety Pak

Medically reviewed on Jan 11, 2018

Dosage form: gel
Ingredients: BENZOCAINE 200mg
Labeler: Gingi-Pak a Division of the Belport
NDC Code: 10129-070

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

GingiCaine Gel, Variety Pak

Active Ingredients

Inactive Ingredients

Warnings

Precautions

Consult a doctor promptly

Allergy alert and contraindications

Purpose

Keep out of reach of children

Dosage and Administration

Indications and Uses

Avoid excessive heat

Gingicaine Gel Variety Pak Labels

GINGICAINE GEL VARIETY PAK 
gingicaine gel variety pak gel
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:10129-070
Route of AdministrationDENTAL, ORAL, PERIODONTALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
BENZOCAINE (BENZOCAINE) BENZOCAINE200 mg
Inactive Ingredients
Ingredient NameStrength
POLYETHYLENE GLYCOL 3350260 mg
POTASSIUM SODIUM SACCHARATE20 mg
POLYETHYLENE GLYCOL 400520 mg
Product Characteristics
Color    Score    
ShapeSize
FlavorCHERRY, STRAWBERRY, BANANA, PINEAPPLE (Pina Colada) , COTTON CANDY, CHOCOLATE (Chocolate Mint) Imprint Code
Contains    
Packaging
#Item CodePackage Description
1NDC:10129-070-016 GEL in 1 BOTTLE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart35606/09/2014
Labeler - Gingi-Pak a Division of the Belport (008480121)

 
Gingi-Pak a Division of the Belport

Further information

Always consult your healthcare provider to ensure the information displayed on this page applies to your personal circumstances.

Hide