Anticavity and sensitive peppermint

907 US VARIANT ANTICAVITY AND SENSITIVE TOOTHPASTE NON FOAMING PEPPERMINT ORAL HUMAN OTC DRUG

Anticavity and sensitive peppermint is an FDA drug label for the active ingredient 907 US VARIANT ANTICAVITY AND SENSITIVE TOOTHPASTE NON FOAMING PEPPERMINT 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 20260630.

Generic name
907 US VARIANT ANTICAVITY AND SENSITIVE TOOTHPASTE NON FOAMING PEPPERMINT
Manufacturer
Dyson Technology Limited
Product type
HUMAN OTC DRUG
Route
ORAL
Dosage form
N/A
NDC
87649-0907
Application
M022
Label effective
20260630

About this product

Anticavity and sensitive peppermint is an FDA-registered drug product whose active ingredient is 907 US VARIANT ANTICAVITY AND SENSITIVE TOOTHPASTE NON FOAMING PEPPERMINT. It is labelled by Dyson Technology Limited taken by oral and marketed as a human otc drug product. Identifiers on file: NDC 87649-0907, application M022, label effective 20260630. 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 907 US VARIANT ANTICAVITY AND SENSITIVE TOOTHPASTE NON FOAMING PEPPERMINT are most often described in connection with: years age, dentist doctor, older apply, least inch, product onto, soft bristle, toothbrush brush, teeth thoroughly. Wording differs between labels, and the full indications section on this page takes precedence when it is present.

Active ingredients

Active ingredients Purpose Sodium fluoride 0.243%... Anticavity (0.14% w/v Fluoride ion) Potassium nitrate 5%.... Antisensitivity

Indications & Usage

Adults and children 12 years of age and older: Apply at least a 1-inch strip of the product onto a soft bristle toothbrush. Brush teeth thoroughly for at least 1 minute twice a day (morning and evening) or as recommended by a dentist or doctor. Make sure to brush all sensitive areas of the teeth. Children under 12 years of age: Consult a dentist or doctor.

Dosage & Administration

Adults and children 12 years of age and older: Apply at least a 1-inch strip of the product onto a soft bristle toothbrush. Brush teeth thoroughly for at least 1 minute twice a day (morning and evening) or as recommended by a dentist or doctor. Make sure to brush all sensitive areas of the teeth.

Warnings

Warnings Keep out of reach of children. If more than used for brushing is accidentally swallowed, get medical help or contact a Poison Control Center right away. Sensitive teeth may indicate a serious problem that may need prompt care by a dentist. See your dentist if the problem persists or worsens. Do not use this product longer than 4 weeks unless recommended by a dentist or doctor.

Frequently asked questions

What is Anticavity and sensitive peppermint used for?
Adults and children 12 years of age and older: Apply at least a 1-inch strip of the product onto a soft bristle toothbrush. Brush teeth thoroughly for at least 1 minute twice a day (morning and evening) or as recommended by a dentist or doctor. Make sure to brush all sensitive areas of the teeth. Children under 12 years of age: Consult a dentist or doctor.

Who makes Anticavity and sensitive peppermint?
Dyson Technology Limited is the labeler of record for Anticavity and sensitive peppermint.

What form does Anticavity and sensitive peppermint 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 and sensitive peppermint 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 and sensitive peppermint 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.