Label: GINGICAINE GEL, CHOCOLATE MINT- gingicaine gel, chocolate mint flavor gel
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Contains inactivated NDC Code(s)
NDC Code(s): 10129-034-01, 10129-034-05 - Packager: Gingi-Pak a Division of the Belport
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated June 29, 2026
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- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Active Ingredient
- Purpose
- Uses
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Warnings
Do not use if you have a history of hypersensitivity to ester–type local anesthetics, not for use with teething or children under 2 years of age.
For topical use only
Methemoglobinemia warning Use of this product may cause methemoglobinemia, a rare but serious condition that must be treated promptly because it reduces the amount of oxygen carried in blood. Consumers are advised to cease use and seek immediate medical attention if they or a child in their care develop:
• Pale, gray, or blue colored skin (cyanosis)
• Headache
• Rapid heart rate
• Shortness of breath • Dizziness or lightheadedness
• Fatigue or lack of energy
Stop use and ask a doctor if (signs of toxicity)
• Sore throat is severe and more than 2 days
• Fever, headache, rash, nausea, or vomiting develops
• Mouth sores do not go away in 7 days
• Irritation, pain, or redness worsens
- Allergy Alert and Contraindications
- Ask a doctor (pharmacist)
- Keep out of reach of children
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Dosage and Administration
Mucosa should be dried prior to application.
Removal of excess saliva with cotton rolls or saliva ejectors will minimize dilution of the local anesthetic.
Sterile cotton or gauze should be used in applying anesthetic to mucosa.
Care must be taken to avoid cross–contamination between patients.
Total dose should not exceed the amount required for anesthesia.
Apply to the affected area. Remain in place for at least 1 minute and then spit out.
• Use up to 4 times a day or as directed by a dentist or doctor.
• This product is for adults and children 2 years of age and older.
- Avoid excessive heat
- Inactive Ingredient
- Gingicaine Mint Chocolate Jar Label
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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 Drug M022 07/06/1993 Labeler - Gingi-Pak a Division of the Belport (008480121)

