United States · FDA National Drug Code directory
PureLife APF
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
- 68987-011_d5f37b59-8611-1f0e-e053-2995a90a3bd9
- Product NDC
- 68987-011
- Form
- GEL
- Composition / generic term
- Sodium Fluoride
- Labeler
- PureLife Dental
- Marketing category
- UNAPPROVED DRUG OTHER
- Marketing start / end (source format)
- 20121218
- Source listing expiry
- 20261231
Source-listed ingredients
- SODIUM FLUORIDE — 5.6 g/454g
These values do not establish equivalence or a dose recommendation.
Packages
- 454 g in 1 BOTTLE, PLASTIC (68987-011-15) · 68987-011-15
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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