Label: GINGICAINE GEL, CHERRY- gingicaine gel, cherry flavor gel
- NDC Code(s): 10129-715-03, 10129-715-05
- 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
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- Active ingredients
- Inactive ingredients
- Precautions
- Warnings
- 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 Cherry Label
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INGREDIENTS AND APPEARANCE
GINGICAINE GEL, CHERRY
gingicaine gel, cherry flavor gelProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:10129-715 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 3350 (UNII: G2M7P15E5P) 260 mg POTASSIUM SODIUM SACCHARATE (UNII: 73U34YC90U) 20 mg POLYETHYLENE GLYCOL 400 (UNII: B697894SGQ) 520 mg Product Characteristics Color red (Cherry flavor) Score Shape Size Flavor Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:10129-715-03 1 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 06/21/1999 2 NDC:10129-715-05 6 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 06/21/1999 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part356 06/21/1999 Labeler - Gingi-Pak a Division of the Belport (008480121)