United States · FDA National Drug Code directory

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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
77782-015_56ac3138-3b52-c419-e063-6294a90a344c
Product NDC
77782-015
Form
GEL, DENTIFRICE
Composition / generic term
SODIUM FLUORIDE
Labeler
MKJ BRANDS LLC
Marketing category
OTC MONOGRAPH DRUG
Marketing start / end (source format)
20250210
Source listing expiry
20271231

Source-listed ingredients

  • SODIUM FLUORIDE — 24 mg/100g

These values do not establish equivalence or a dose recommendation.

Packages

  • 113 g in 1 BOTTLE (77782-015-13) · 77782-015-13
  • 141 g in 1 BOTTLE (77782-015-14) · 77782-015-14

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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