Anticavity mouth rinse Low-foaming Spearmint
Anticavity mouth rinse Low-foaming Spearmint is an FDA drug label for the active ingredient 718 US VARIANT ANTICAVITY MOUTH RINSE LOW-FOAMING SPEARMINT manufactured by Dyson Technology Limited administered by ORAL. 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 20260626.
- Generic name
- 718 US VARIANT ANTICAVITY MOUTH RINSE LOW-FOAMING SPEARMINT
- Manufacturer
- Dyson Technology Limited
- Product type
- HUMAN OTC DRUG
- Route
- ORAL
- Dosage form
- N/A
- NDC
- 87649-7180
- Application
- M021
- Label effective
- 20260626
About this product
Anticavity mouth rinse Low-foaming Spearmint is an FDA-registered drug product whose active ingredient is 718 US VARIANT ANTICAVITY MOUTH RINSE LOW-FOAMING SPEARMINT. It is labelled by Dyson Technology Limited taken by oral and marketed as a human otc drug product. Identifiers on file: NDC 87649-7180, application M021, label effective 20260626. 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 718 US VARIANT ANTICAVITY MOUTH RINSE LOW-FOAMING SPEARMINT are most often described in connection with: years age, directions adults, twice day, toothpaste vigorously, swish millilitres, eat drink, rinsing instruct, habits minimize. Wording differs between labels, and the full indications section on this page takes precedence when it is present.
Active ingredients
Indications & Usage
Directions Adults and children 6 years of age and older Use twice a day after brushing your teeth with a toothpaste. • vigorously swish 10 millilitres of rinse between your teeth for 1 minute and then spit out. • do not swallow the rinse. • do not eat or drink for 30 minutes after rinsing. • instruct children under 12 years of age in good rinsing habits (to minimize swallowing). • supervise children as necessary until capable of using without supervision. • children under 6 years of age: consult a dentist or doctor.
Dosage & Administration
Use twice a day after brushing your teeth with a toothpaste. • vigorously swish 10 millilitres of rinse between your teeth for 1 minute and then spit out. • do not swallow the rinse. • do not eat or drink for 30 minutes after rinsing. • instruct children under 12 years of age in good rinsing habits (to minimize swallowing). • supervise children as necessary until capable of using without supervision. • children under 6 years of age: consult a dentist or doctor.
Warnings
Warning Keep out of the reach of children. If more than used for rinsing is accidentally swallowed, get medical help or contact a Poison Control Center right away.
Frequently asked questions
What is Anticavity mouth rinse Low-foaming Spearmint used for?
Directions Adults and children 6 years of age and older Use twice a day after brushing your teeth with a toothpaste. • vigorously swish 10 millilitres of rinse between your teeth for 1 minute and then spit out. • do not swallow the rinse. • do not eat or drink for 30 minutes after rinsing. • instruct children under 12 years of age in good rinsing habits (to minimize swallowing). • supervise …
Who makes Anticavity mouth rinse Low-foaming Spearmint?
Dyson Technology Limited is the labeler of record for Anticavity mouth rinse Low-foaming Spearmint.
What form does Anticavity mouth rinse Low-foaming Spearmint come in?
administered by oral. Strengths and pack sizes vary by label, so compare the NDC on your pack with the identifier listed on this page.
Is Anticavity mouth rinse Low-foaming Spearmint 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 Anticavity mouth rinse Low-foaming Spearmint 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.