Home NDC 37000-868 Crest
Product NDC 37000-868
11-digit product format 370000868
Labeler code 37000
Product ID 37000-868_4aa60484-78be-875c-e063-6294a90ab84f
Type HUMAN OTC DRUG
Nonproprietary name Sodium Fluoride
Dosage form PASTE, DENTIFRICE
Route DENTAL
Labeler The Procter & Gamble Manufacturing Company
Application M021
Marketing category OTC MONOGRAPH DRUG
Marketing start 2015-03-09
Substance SODIUM FLUORIDE
Active strength 1.5 mg/g
NDC exclude flag No
Listing certified through 2027-12-31
Current FDA listing Yes
Observed NDC auxiliary status history# This history shows the information present in each captured FDA auxiliary file. It is not a continuous regulatory timeline, and a missing record does not establish a status.
Historic NDC status page 1 of 1 · 3 matching rows.
View current auxiliary records. · View the auxiliary file history.
Captured / source date, Dataset, Scope table Captured / source date Dataset Scope Product NDC Package NDC Code Status Reporting period Archive Snapshot Source SHA-256 2025-12-14 17:58 UTC · source 2025-12-05 excluded package package 37000-868 37000-868-02 D Discontinued by firm excluded / ndc_excluded.zip d630ba8d3edf…732f749b63fb…2025-12-14 17:58 UTC · source 2025-12-05 excluded package package 37000-868 37000-868-57 D Discontinued by firm excluded / ndc_excluded.zip d630ba8d3edf…732f749b63fb…2025-12-14 17:58 UTC · source 2025-12-05 excluded package package 37000-868 37000-868-06 D Discontinued by firm excluded / ndc_excluded.zip d630ba8d3edf…732f749b63fb…
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.
Additional Listing Data#
Finished product Yes
Brand name base Crest
Brand name suffix Fresh and White
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength SODIUM FLUORIDE 1.5 mg/g
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 8ZYQ1474W7 Internal UNII lookup
Harmonized RxCUI identifiers# RxCUI identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 891775 Internal RxNorm lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
FDA-Initiated Inactive NDC Indexing# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 37000-868-02 CrestFresh and White 82 g in 1 TUBE PASTE, DENTIFRICE 82 12 37000-868-02 CrestFresh and White 1 in 1 CARTON PASTE, DENTIFRICE 1 12 37000-868-06 CrestFresh and White 1 in 1 CARTON PASTE, DENTIFRICE 1 12 37000-868-06 CrestFresh and White 181 g in 1 TUBE PASTE, DENTIFRICE 181 12 37000-868-24 CrestFresh and White 68 g in 1 TUBE PASTE, DENTIFRICE 68 12 37000-868-24 CrestFresh and White 1 in 1 CARTON PASTE, DENTIFRICE 1 12 37000-868-57 CrestFresh and White 161 g in 1 TUBE PASTE, DENTIFRICE 161 12 37000-868-57 CrestFresh and White 1 in 1 CARTON PASTE, DENTIFRICE 1 12
DailyMed Socrata Ingredients# Ingredient, Type, UNII table Ingredient Type UNII DailyMed label SPL version Uploaded Sodium Fluoride ACTIVE INGREDIENT 8ZYQ1474W7 CREST FRESH AND WHITE (SODIUM FLUORIDE) PASTE, DENTIFRICE [THE PROCTER & GAMBLE MANUFACTURING COMPANY] 1 Fluoride Ion ACTIVE MOIETY Q80VPU408O CREST FRESH AND WHITE (SODIUM FLUORIDE) PASTE, DENTIFRICE [THE PROCTER & GAMBLE MANUFACTURING COMPANY] 1 CARBOXYMETHYLCELLULOSE SODIUM, UNSPECIFIED FORM INACTIVE INGREDIENT K679OBS311 CREST FRESH AND WHITE (SODIUM FLUORIDE) PASTE, DENTIFRICE [THE PROCTER & GAMBLE MANUFACTURING COMPANY] 1 HYDRATED SILICA INACTIVE INGREDIENT Y6O7T4G8P9 CREST FRESH AND WHITE (SODIUM FLUORIDE) PASTE, DENTIFRICE [THE PROCTER & GAMBLE MANUFACTURING COMPANY] 1 SACCHARIN SODIUM INACTIVE INGREDIENT SB8ZUX40TY CREST FRESH AND WHITE (SODIUM FLUORIDE) PASTE, DENTIFRICE [THE PROCTER & GAMBLE MANUFACTURING COMPANY] 1 SODIUM LAURYL SULFATE INACTIVE INGREDIENT 368GB5141J CREST FRESH AND WHITE (SODIUM FLUORIDE) PASTE, DENTIFRICE [THE PROCTER & GAMBLE MANUFACTURING COMPANY] 1 SODIUM PHOSPHATE INACTIVE INGREDIENT SE337SVY37 CREST FRESH AND WHITE (SODIUM FLUORIDE) PASTE, DENTIFRICE [THE PROCTER & GAMBLE MANUFACTURING COMPANY] 1 SORBITOL INACTIVE INGREDIENT 506T60A25R CREST FRESH AND WHITE (SODIUM FLUORIDE) PASTE, DENTIFRICE [THE PROCTER & GAMBLE MANUFACTURING COMPANY] 1 TITANIUM DIOXIDE INACTIVE INGREDIENT 15FIX9V2JP CREST FRESH AND WHITE (SODIUM FLUORIDE) PASTE, DENTIFRICE [THE PROCTER & GAMBLE MANUFACTURING COMPANY] 1 WATER INACTIVE INGREDIENT 059QF0KO0R CREST FRESH AND WHITE (SODIUM FLUORIDE) PASTE, DENTIFRICE [THE PROCTER & GAMBLE MANUFACTURING COMPANY] 1
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 37000-868 CREST FRESH AND WHITE (SODIUM FLUORIDE) PASTE, DENTIFRICE [THE PROCTER & GAMBLE MANUFACTURING COMPANY] 9 Current NDC, Legacy NDC, 8 package rows 20250110_8693fa6d-e9c9-4cb7-bd3d-8ad87a7bb77e.zip
openFDA label cross-check# OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
Matched openFDA labels page 5 of 50 · 995 matching rows.
DailyMed RxNorm Mappings# Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 37000-868-02 37000086802 1 TUBE in 1 CARTON (37000-868-02) > 82 g in 1 TUBE 1 tube 2015-03-09 2021-12-01 No No Current 37000-868-06 37000086806 1 TUBE in 1 CARTON (37000-868-06) > 181 g in 1 TUBE 1 tube 2015-03-09 0000-00-00 No No Current 37000-868-24 37000086824 1 TUBE in 1 CARTON (37000-868-24) / 68 g in 1 TUBE 1 tube 2019-09-10 0000-00-00 No No Current 37000-868-57 37000086857 1 TUBE in 1 CARTON (37000-868-57) > 161 g in 1 TUBE 1 tube 2015-03-09 0000-00-00 No No Current