United States · FDA National Drug Code directory

Denta 5000 Plus

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
16571-814_82dc4f9f-0dc5-46f8-8deb-3966669470cd
Product NDC
16571-814
Form
CREAM
Composition / generic term
Sodium fluoride
Labeler
Rising Pharma Holdings, Inc.
Marketing category
UNAPPROVED DRUG OTHER
Marketing start / end (source format)
20230703
Source listing expiry
20261231

Source-listed ingredients

  • SODIUM FLUORIDE — 1.1 g/100g

These values do not establish equivalence or a dose recommendation.

Packages

  • 51 g in 1 TUBE (16571-814-50) · 16571-814-50

Source and coverage

Open FDA National Drug Code directory

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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Denta 5000 Plus — United States | Molindra Medicines