FDA.reportPublic FDA data

Kids Crest

Product NDC
37000-896
Requested package NDC
37000-896-36
11-digit product format
370000896
Labeler code
37000
Product ID
37000-896_bb26208c-64c4-f440-e053-2995a90ad557
Type
HUMAN OTC DRUG
Nonproprietary name
Sodium Fluoride
Dosage form
RINSE
Route
ORAL
Labeler
The Procter & Gamble Manufacturing Company
Application
part355
Marketing category
OTC MONOGRAPH FINAL
Marketing start
2017-12-15
Marketing end
0000-00-00
Substance
SODIUM FLUORIDE
Active strength
0 mg/mL
NDC exclude flag
No
Listing certified through
2022-12-31
Current FDA listing
Historical FDA.report record

NDC auxiliary status#

These records are reproduced from FDA’s unfinished, excluded, and compounder listings. They describe what appeared in the source files; a missing record does not establish a regulatory status. View all current auxiliary records, including entries without an NDC. · View the auxiliary file history.

Current NDC status page 1 of 1 · 1 matching rows.

Dataset, Scope, Product NDC table
DatasetScopeProduct NDCPackage NDCCodeStatusReporting periodSource date
excluded packagepackage37000-89637000-896-36DDiscontinued by firm2026-10-05

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 dateDatasetScopeProduct NDCPackage NDCCodeStatusReporting periodArchiveSnapshotSource SHA-256
2025-12-14 17:58 UTC · source 2025-12-05excluded packagepackage37000-89637000-896-36DDiscontinued by firmexcluded / ndc_excluded.zipd630ba8d3edf…732f749b63fb…
2025-08-27 00:01 UTC · source 2025-08-26excluded packagepackage37000-89637000-896-36DDiscontinued by firmexcluded / ndc_excluded.zipf5e01cc5f278…a2eaf40c39c3…
2025-01-11 03:41 UTC · source 2025-01-10excluded packagepackage37000-89637000-896-36UExcluded because listing certification expiredexcluded / ndc_excluded.zip0efc9e666f02…f202fb6c5f17…

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Related label table
NDCEffectiveRelated label
37000-896-052023-05-18Kid's Crest® Anticavity Fluoride Rinse Strawberry Rush™
37000-896-362023-05-18Kid's Crest® Anticavity Fluoride Rinse Strawberry Rush™
37000-896-052023-01-30Kid's Crest® Anticavity Fluoride Rinse Strawberry Rush™
37000-896-362023-01-30Kid's Crest® Anticavity Fluoride Rinse Strawberry Rush™
37000-896-052021-02-12Kid's Crest® Anticavity Fluoride Rinse Strawberry Rush™
37000-896-362021-02-12Kid's Crest® Anticavity Fluoride Rinse Strawberry Rush™
37000-896-052021-01-29Kid's Crest® Anticavity Fluoride Rinse Strawberry Rush™
37000-896-362021-01-29Kid's Crest® Anticavity Fluoride Rinse Strawberry Rush™

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
37000-896KIDS CREST STRAWBERRY RUSH (SODIUM FLUORIDE) RINSE [THE PROCTER & GAMBLE MANUFACTURING COMPANY]6Legacy NDC20250114_60a2e223-9f48-2f3f-e053-2991aa0abf1c.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
37000-896-363700008963636 mL in 1 BOTTLE, PLASTIC (37000-896-36) 36 ml2019-01-280000-00-00NoNoCurrent