DailyMed label

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DailyMed label · The Procter & Gamble Manufacturing Company · version 1

Key facts

Product Crest Premium Plus
Labeler The Procter & Gamble Manufacturing Company
Document type HUMAN OTC DRUG LABEL
Active ingredients SODIUM FLUORIDE
Active ingredient UNIIs 8ZYQ1474W7
Application number M021
Route DENTAL
NDC package codes 84126-662-52
Effective date Jun 24, 2026
Set ID 5504ec96-aae1-f5f9-e063-6294a90ad8bb

At a glance

  • 1–9 NDC package codes
  • 1–9 Active ingredients
  • None Manufacturing establishments listed

Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.

About DailyMed drug labels

DailyMed publishes the structured product labeling (SPL) that companies submit to the FDA, including package NDCs, ingredients and the establishments that make each product.

Source: U.S. National Library of Medicine (NLM), DailyMed · Source date:

Browse all DailyMed drug labels