Zap Neutral
Zap Neutral is an FDA drug label for the active ingredient SODIUM FLUORIDE manufactured by Crosstex International Inc. 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 20220119.
- Generic name
- SODIUM FLUORIDE
- Manufacturer
- Crosstex International Inc.
- Product type
- HUMAN PRESCRIPTION DRUG
- Route
- DENTAL
- Dosage form
- N/A
- NDC
- 24794-108
- Application
- N/A
- Label effective
- 20220119
About this product
Zap Neutral is an FDA-registered drug product whose active ingredient is SODIUM FLUORIDE. It is labelled by Crosstex International Inc. taken by dental and marketed as a human prescription drug product. Identifiers on file: NDC 24794-108, label effective 20220119. It is one of 263 FDA drug label records sharing the active ingredient SODIUM FLUORIDE. 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 SODIUM FLUORIDE are most often described in connection with: prescription fluoride, treatment gel, help prevent, dental decay. Wording differs between labels, and the full indications section on this page takes precedence when it is present.
Indications & Usage
Indications and Usage: This is a prescription fluoride treatment gel used to help prevent dental decay.
Dosage & Administration
Dosage and Administration: Shake lightly before use. This is a four minute topical fluoride gel for in-office patient use. It is normally used as a preventative caries treatment two times a year. 1. After thorough prophylaxsis, fill two single or one dual tray, one third full with gel. Air dry teeth and insert trays into the mouth. 2. Instruct patient to bite down lightly but firmly four minutes. 3. Remove trays. Instruct patient to expectorate any excess gel and not to eat or drink for at least 30 minutes.
Warnings
Warnings: Keep out of reach of children. Do not swallow. If product is accidentally swallowed in quantities greater than would normally occur with a treatment gel, seek medical help or contact a Poison Control Center right away. This product contains a concentrated fluoride amount and is available by prescription only. It should be used under professional supervision.
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View labelHow products containing SODIUM FLUORIDE compare
FDA lists 263 drug label records with SODIUM FLUORIDE as the active ingredient. The most common dosage forms and the manufacturers with the most records are summarised below; strengths, pack sizes and inactive ingredients can still differ between apparently similar products.
| Dosage form | Products | Manufacturer | Products |
|---|---|---|---|
| — | — | Colgate-Palmolive Company | 34 |
| — | — | The Procter & Gamble Manufacturing Company | 25 |
| — | — | Church & Dwight Co., Inc. | 14 |
| — | — | Burkhart Dental Supply Inc | 12 |
| — | — | Dharma Research, inc. | 12 |
Frequently asked questions
What is Zap Neutral used for?
Indications and Usage: This is a prescription fluoride treatment gel used to help prevent dental decay.
Who makes Zap Neutral?
Crosstex International Inc. is the labeler of record for Zap Neutral. 263 FDA label records share the active ingredient SODIUM FLUORIDE, so generic and branded versions may come from different companies; the manufacturer named on your pack is the one that matters for any enquiry.
What form does Zap Neutral 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 Zap Neutral prescription or over-the-counter?
The FDA label for this product is recorded as human prescription drug. Marketing status can differ between strengths and countries, so check the dispensing rules where you live.
Are there other products containing SODIUM FLUORIDE?
Yes. 263 FDA drug label records list SODIUM FLUORIDE as the active ingredient. Products with the same active ingredient can usually be substituted only when a prescriber or pharmacist confirms it is appropriate.
Has Zap Neutral 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.