Label: GINGICAINE GEL, CHOCOLATE MINT- gingicaine gel, chocolate mint flavor gel
- NDC Code(s): 10129-034-01, 10129-034-05
- Packager: Gingi-Pak a Division of the Belport
- Category: HUMAN OTC DRUG LABEL
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.
Drug Label Information
Updated December 9, 2021
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- Official Label (Printer Friendly)
- Active Ingredient
- Inactive Ingredient
- 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
- Warnings
- Mint chocolate flavor
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INGREDIENTS AND APPEARANCE
GINGICAINE GEL, CHOCOLATE MINT
gingicaine gel, chocolate mint flavor gelProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:10129-034 Route of Administration ORAL, PERIODONTAL, DENTAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength BENZOCAINE (UNII: U3RSY48JW5) (BENZOCAINE - UNII:U3RSY48JW5) BENZOCAINE 200 mg Inactive Ingredients Ingredient Name Strength POLYETHYLENE GLYCOL 3350 (UNII: G2M7P15E5P) 260 mg POLYETHYLENE GLYCOL 400 (UNII: B697894SGQ) 520 mg POTASSIUM SODIUM SACCHARATE (UNII: 73U34YC90U) 20 mg Product Characteristics Color Score Shape Size Flavor CHOCOLATE (chocolate mint) Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:10129-034-01 1 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 07/06/1993 2 NDC:10129-034-05 6 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 07/06/1993 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part356 07/06/1993 Labeler - Gingi-Pak a Division of the Belport (008480121)