United States · FDA National Drug Code directory

Crest 3D White Brilliance Pro Ultra White

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
69423-760_49ee5903-6e3a-c329-e063-6294a90a3be4
Product NDC
69423-760
Form
PASTE, DENTIFRICE
Composition / generic term
Sodium monofluorophosphate
Labeler
The Procter & Gamble Manufacturing Company
Marketing category
OTC MONOGRAPH DRUG
Marketing start / end (source format)
20230110
Source listing expiry
20271231

Source-listed ingredients

  • SODIUM MONOFLUOROPHOSPHATE — 1.7 mg/g

These values do not establish equivalence or a dose recommendation.

Packages

  • 1 TUBE in 1 CARTON (69423-760-30) / 85 g in 1 TUBE · 69423-760-30
  • 1 TUBE in 1 CARTON (69423-760-38) / 107 g in 1 TUBE · 69423-760-38

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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Crest 3D White Brilliance Pro Ultra White — United States | Molindra Medicines