Label: GINGICAINE LIQUID, CHERRY- gingicaine liquid, cherry flavor liquid
- NDC Code(s): 10129-720-03, 10129-720-05
- Packager: Gingi-Pak a Division of the Belport
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: OTC monograph not final
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
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- 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
- Liquid cherry label
-
INGREDIENTS AND APPEARANCE
GINGICAINE LIQUID, CHERRY
gingicaine liquid, cherry flavor liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:10129-720 Route of Administration DENTAL, ORAL, PERIODONTAL 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 400 (UNII: B697894SGQ) 785 mg POTASSIUM SODIUM SACCHARATE (UNII: 73U34YC90U) 20 mg Product Characteristics Color Score Shape Size Flavor CHERRY (Color red) Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:10129-720-03 1 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 07/19/1999 2 NDC:10129-720-05 6 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 06/10/2014 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part356 07/19/1999 Labeler - Gingi-Pak a Division of the Belport (008480121)
