# Freshen Up Vanilla Mint

NDC: 87846-006
Generic name: SODIUM FLUORIDE
Labeler / Manufacturer: Dabur India Limited
Product type: HUMAN OTC DRUG
Marketing category: OTC monograph drug
Dosage form: GEL, DENTIFRICE
Routes: DENTAL
Marketing started: 20260521

FDA application: M021

## Active ingredients

- SODIUM FLUORIDE: .24 g/100g

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"87846-006"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=87846-006
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=56aad223-db88-7cf6-e063-6394a90a6b72