Gingicaine Gel Strawberry
Gingicaine Gel Strawberry is an FDA drug label for the active ingredient GINGICAINE GEL STRAWBERRY FLAVOR manufactured by Gingi-Pak a Division of the Belport administered by DENTAL. This page reproduces the FDA-approved indications and usage, dosage, contraindications, warnings, and adverse reactions exactly as published in the drug label. Data source: openFDA (U.S. FDA), label effective 20260501.
- Generic name
- GINGICAINE GEL STRAWBERRY FLAVOR
- Manufacturer
- Gingi-Pak a Division of the Belport
- Product type
- HUMAN OTC DRUG
- Route
- DENTAL
- Dosage form
- N/A
- NDC
- 10129-036
- Application
- M022
- Label effective
- 20260501
About this product
Gingicaine Gel Strawberry is an FDA-registered drug product whose active ingredient is GINGICAINE GEL STRAWBERRY FLAVOR. It is labelled by Gingi-Pak a Division of the Belport taken by dental and marketed as a human otc drug product. Identifiers on file: NDC 10129-036, application M022, label effective 20260501. This page reproduces the FDA-approved label text so you can check what a product is, who makes it and how it is supplied before discussing it with a pharmacist or prescriber.
What it is used for
Across FDA labelling, products containing GINGICAINE GEL STRAWBERRY FLAVOR are most often described in connection with: orthodontic appliances, usage section, anesthesia mucous, membrane oropharynx, temporarily relieves, pain discomfort, caused minor, dental procedures. Wording differs between labels, and the full indications section on this page takes precedence when it is present.
Active ingredients
Indications & Usage
Indications and usage section For anesthesia of mucous membrane of oropharynx. Temporarily relieves pain or discomfort caused by minor dental procedures, orthodontic appliances, teething, canker sores, cold sores, fever blisters, minor injury of the mouth or gums, and irritations caused by dentures or orthodontic appliances.
Dosage & Administration
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 daily or as directed by a dentist or doctor. • Do not exceed recommended dosage. • This product is for adults and children 2 years of age and older. • Children under 2 years of age should consult a dentist or a doctor.
Warnings
Precaution Section Dentists should avoid application to severely traumatized, infected mucosal areas or areas of the posterior pharynx that might obtund protective reflexes. Local anesthetics should be used with caution in patients with known drug sensitivities, particularly those known to be allergic to ester-type anesthetics (procaine, benzocaine, tetracaine). Dentists should avoid contact with all local anesthetics to avoid possible sensitization.
Frequently asked questions
What is Gingicaine Gel Strawberry used for?
Indications and usage section For anesthesia of mucous membrane of oropharynx. Temporarily relieves pain or discomfort caused by minor dental procedures, orthodontic appliances, teething, canker sores, cold sores, fever blisters, minor injury of the mouth or gums, and irritations caused by dentures or orthodontic appliances.
Who makes Gingicaine Gel Strawberry?
Gingi-Pak a Division of the Belport is the labeler of record for Gingicaine Gel Strawberry.
What form does Gingicaine Gel Strawberry come in?
administered by dental. Strengths and pack sizes vary by label, so compare the NDC on your pack with the identifier listed on this page.
Is Gingicaine Gel Strawberry prescription or over-the-counter?
The FDA label for this product is recorded as human otc drug. Marketing status can differ between strengths and countries, so check the dispensing rules where you live.
Has Gingicaine Gel Strawberry been recalled?
No FDA recall record in our database matches this product name or manufacturer. Recall data is updated periodically, so a very recent notice may not appear here yet.
Where does this information come from?
All content is reproduced from FDA Structured Product Labelling data via openFDA. It is provided for identification and reference only and is not medical advice.
This page reproduces FDA Structured Product Labelling data for identification and reference. It is not medical advice, does not diagnose or treat any condition, and does not sell or price any medicine.