NDC 69367-318
Sodium Fluoride and Potassium Nitrate 5.8 mg per 1 mL / 57.5 mg per 1 mL gel
On the label: Westminster Pharmaceuticals, LLC.
Where it's made
This label doesn't name the factory that makes the drug. Companies don't have to print it on the label. The maker's name is often on the stock bottle your pharmacy used; you can ask the pharmacist. See the plants Westminster Pharmaceuticals, LLC names for other drugs.
Product details
- Generic drug
- Fluoride Ion and Nitrate Ion: every company that makes it
- Form
- gel, dental
- Strength
- 5.8 mg per 1 mL / 57.5 mg per 1 mL
- Approval
- UNAPPROVED DRUG OTHER
- On the market since
- Jun 15, 2022
- Package NDCs
69367-318-01- Official label
- DailyMed (National Library of Medicine), updated Apr 18, 2024
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