United States · FDA National Drug Code directory
Auraglow Whitening
A source-listed medicine record.
Factual source checks only. This page is not a clinically reviewed monograph. Historical or discontinued records may be included; listing does not confirm approval, current availability or pharmacy stock.
Medicine identity
- Source reference
- 81740-003_3f72b20e-32ad-468c-a67b-ff438c3a8396
- Product NDC
- 81740-003
- Form
- PASTE, DENTIFRICE
- Composition / generic term
- SODIUM FLUORIDE
- Labeler
- Auraglow LLC
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start / end (source format)
- 20251020
- Source listing expiry
- 20261231
Source-listed ingredients
- SODIUM FLUORIDE — 2.3 mg/g
These values do not establish equivalence or a dose recommendation.
Packages
- 1 TUBE in 1 CARTON (81740-003-03) / 113 g in 1 TUBE · 81740-003-03
Source and coverage
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Snapshot retrieved: 2026-09-17. This is the acquisition date, not a medical review date.
Clinical information, images and comparisons appear only when separately reviewed for this record. Coverage may be incomplete. Ask a pharmacist or clinician about your treatment.
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