Beyond Activated Coconut Charcoal and Sea Salt
Beyond Activated Coconut Charcoal and Sea Salt is an FDA drug label for the active ingredient SODIUM FLUORIDE manufactured by Beyond 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 20231128.
- Generic name
- SODIUM FLUORIDE
- Manufacturer
- Beyond International Inc
- Product type
- HUMAN OTC DRUG
- Route
- DENTAL
- Dosage form
- N/A
- NDC
- 42199-008
- Application
- M021
- Label effective
- 20231128
About this product
Beyond Activated Coconut Charcoal and Sea Salt is an FDA-registered drug product whose active ingredient is SODIUM FLUORIDE. It is labelled by Beyond International Inc taken by dental and marketed as a human otc drug product. Identifiers on file: NDC 42199-008, application M021, label effective 20231128. 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: aids prevention, dental cavities. Wording differs between labels, and the full indications section on this page takes precedence when it is present.
Active ingredients
Indications & Usage
Uses Aids in prevention of dental cavities.
Dosage & Administration
Directions adults and children 2 years of age and older: brush teeth thoroughly, preferably after each meal or at least twice a day, or as directed by a dentist or doctor. instruct children under 6 years of age in good brushing or rinsing habits (to minimize swallowing) supervise children as necessary until good habits are established children under 2 years: ask a dentist or doctor
Warnings
Warnings
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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 Beyond Activated Coconut Charcoal and Sea Salt used for?
Uses Aids in prevention of dental cavities.
Who makes Beyond Activated Coconut Charcoal and Sea Salt?
Beyond International Inc is the labeler of record for Beyond Activated Coconut Charcoal and Sea Salt. 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 Beyond Activated Coconut Charcoal and Sea Salt 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 Beyond Activated Coconut Charcoal and Sea Salt 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.
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 Beyond Activated Coconut Charcoal and Sea Salt 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.