Gingicaine Liquid, Cherry
Product Images NDC 10129-720

Product Visual Gallery

This gallery contains 15 technical images submitted to the FDA as part of the official labeling for Gingicaine Liquid, Cherry (NDC 10129-720). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Gingi-pak A Division Of The Belport, these visuals offer a comprehensive scientific overview of the product's physical and chemical identity, aiding pharmacists and researchers in product verification and study.

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Keep Out Of Reach Of Children (Children Page 001)

This text is a warning for the use of Gingicaine Gel product and advises to keep it away from children. It also provides guidance to contact the doctor immediately in case of ingestion or swallowing of the product by a child.*

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Contraindications

This text is a warning about the contraindications of using a product containing ester-type local anesthetics. It advises against using the product for teething or in infants and children younger than 2 years. Additionally, it warns against using the product in patients with a history of hypersensitivity to ester-type local anesthetics.*

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Gingicaine Cherry Liquid Jar Label

This is a Drug Facts sheet for GINGICaine, which is a 20% Benzocaine Oral Anesthetic used to reduce pain or discomfort caused by minor dental procedures, minor gum injuries, canker sores, sore throat, minor mouth, or gum irritations caused by dentures or orthodontic appliances. This product can cause methemoglobinemia, which reduces the amount of oxygen carried in blood, and doctors recommend avoiding contact with all local anesthetics to avoid possible sensitization. It should not be used in children under 2 years of age, for teething, or in patients with a history of hypersensitivity to ester-type local anesthetics. The product should not be used in infants and children younger than 2 years. If sore throat is severe, persists for more than 2 days, is accompanied or followed by fever, headache, rash, nausea, or vomiting, a doctor should be consulted immediately.*

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Inactive Ingredient (Gingicaine Liquid Inactive Ingredient)

Polyethylene Glycol 400 is a commonly used chemical compound that is used as a lubricant, solvent, surfactant, and plasticizer in a variety of industrial and pharmaceutical applications. It is a clear, odorless liquid that is soluble in water, alcohol, and ether. Potassium Sodium Saccharate is not-readable.*

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Active Ingredient (Gingicaine Active Ingredients 001)

Benzocaine 20% w/v is an active ingredient used as an oral anesthetic.*

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Allergy Alert (Gingicaine Allergy Alert 001)

This is a warning message that advises against the use of a particular product if the person has a history of allergy to any "caine" local anesthetics or FD&C Red #40.*

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Avoid Excessive Heat (Gingicaine Avoid Excessive Heat)

This is a warning to avoid exposing the object to temperatures exceeding 40 °C (104 °F) to prevent damage or malfunction.*

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Consult A Doctor Promptly (Gingicaine Consult A Doctor)

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Dosage And Administration 001 (Gingicaine Dosage And Admin 001)

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Dosage And Administration 002 (Gingicaine Dosage And Admin 002)

This is a set of instructions on how to properly use local anesthetic. It advises using cotton rolls or saliva ejectors to reduce dilution of the anesthetic, and sterile cotton or gauze to apply it to the mucosa. Care should be taken to avoid cross-contamination between patients, and the total dose should not exceed what is necessary for anesthesia. The anesthetic should be applied to the affected area for at least one minute and then spit out. It can be used up to four times a day or as directed by a dentist or doctor, but the recommended dosage should not be exceeded. This product is intended for adults and children aged two and up, but children under two should seek advice from a dentist or doctor.*

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Indications (Gingicaine Indications 001)

This text describes the different uses of an anesthesia for mucous membranes of the oropharynx. It mentions that it can help minimize pain during ulcers, needle puncture, scaling procedures, application of matrix bands and taking impressions or intraoral radiographs for patients with a strong gag reflex.*

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Precautions (Gingicaine Precaution 001)

This text provides precautions for dentists regarding the use of local anesthetics. Dentists should be cautious when applying the anesthetics to infected or severely traumatized mucosal areas or to the posterior pharynx where protective reflexes may be affected. Patients with known drug sensitivities, especially those allergic to ester-type anesthetics like procaine, benzocaine, and tetracaine, should be given anesthetics with caution. The text also suggests that dentists should avoid contact with all local anesthetics to prevent possible sensitization.*

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Uses (Gingicaine Uses 001)

This text describes the uses of a product that helps to reduce pain or discomfort caused by minor dental procedures, minor gum injury, canker sores, sore throat, and minor mouth or gum irritations caused by dentures or orthodontic appliances.*

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Purpose (Purpose Page 001)

Gingicaine Gel is a numbing cream applied by dentists before administering injections. The gel is typically applied directly to the patient's gum.*

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Warnings

This text is a warning label for a product. It states that the product is for external use only and may cause a serious condition called methemoglobinemia, which reduces the amount of oxygen in the blood. It advises to stop using the product and seek immediate medical attention if symptoms such as pale, gray or blue-colored skin, headache, rapid heart rate, shortness of breath, dizziness or lightheadedness, fatigue or lack of energy develop. The product should not be used in children under 2 years of age.*

* About these descriptions: Image descriptions on this page are generated by automated AI analysis of the product label images from the manufacturer's FDA label submission (SPL). They are provided for reference only and may contain errors or omissions. Always rely on the printed label itself and the official FDA labeling, and consult a pharmacist or healthcare professional with any questions about this product.