Home NDC 52410-9005 Medpride
Product NDC 52410-9005
11-digit product format 524109005
Labeler code 52410
Product ID 52410-9005_2bd54896-ace8-e65b-e063-6294a90a8cd4
Type HUMAN OTC DRUG
Nonproprietary name Sodium monofluorophosphate
Dosage form PASTE, DENTIFRICE
Route DENTAL
Labeler Shield Line LLC
Application M021
Marketing category OTC MONOGRAPH DRUG
Marketing start 2013-05-27
Substance SODIUM MONOFLUOROPHOSPHATE
Active strength 7.6 mg/g
NDC exclude flag No
Listing certified through 2026-12-31
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 2024-03-11 06:39 UTC · source 2024-03-08 excluded product product 52410-9005 I Inactivated by FDA excluded / ndc_excluded.zip 1332a3947898…d4bfe170f9cd…2024-03-11 06:39 UTC · source 2024-03-08 excluded package package 52410-9005 52410-9005-4 I Inactivated by FDA excluded / ndc_excluded.zip 1332a3947898…d4bfe170f9cd…2024-03-11 06:39 UTC · source 2024-03-08 excluded package package 52410-9005 52410-9005-3 I Inactivated by FDA excluded / ndc_excluded.zip 1332a3947898…d4bfe170f9cd…
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 Medpride
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength SODIUM MONOFLUOROPHOSPHATE 7.6 mg/g
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination C810JCZ56Q Internal UNII lookup
Harmonized RxCUI identifiers# RxCUI identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 545626 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 52410-9005-3 Medpride 42.5 g in 1 TUBE PASTE, DENTIFRICE 42.5 5 52410-9005-4 Medpride 78 g in 1 TUBE PASTE, DENTIFRICE 78 5
DailyMed Socrata Ingredients# Ingredient, Type, UNII table Ingredient Type UNII DailyMed label SPL version Uploaded SODIUM MONOFLUOROPHOSPHATE ACTIVE INGREDIENT C810JCZ56Q MEDPRIDE (SODIUM MONOFLUOROPHOSPHATE ) PASTE, DENTIFRICE [SHIELD LINE LLC ] 1 FLUORIDE ION ACTIVE MOIETY Q80VPU408O MEDPRIDE (SODIUM MONOFLUOROPHOSPHATE ) PASTE, DENTIFRICE [SHIELD LINE LLC ] 1 CALCIUM CARBONATE INACTIVE INGREDIENT H0G9379FGK MEDPRIDE (SODIUM MONOFLUOROPHOSPHATE ) PASTE, DENTIFRICE [SHIELD LINE LLC ] 1 CARBOXYMETHYLCELLULOSE SODIUM INACTIVE INGREDIENT K679OBS311 MEDPRIDE (SODIUM MONOFLUOROPHOSPHATE ) PASTE, DENTIFRICE [SHIELD LINE LLC ] 1 HYDRATED SILICA INACTIVE INGREDIENT Y6O7T4G8P9 MEDPRIDE (SODIUM MONOFLUOROPHOSPHATE ) PASTE, DENTIFRICE [SHIELD LINE LLC ] 1 METHYLPARABEN SODIUM INACTIVE INGREDIENT CR6K9C2NHK MEDPRIDE (SODIUM MONOFLUOROPHOSPHATE ) PASTE, DENTIFRICE [SHIELD LINE LLC ] 1 PROPYLPARABEN INACTIVE INGREDIENT Z8IX2SC1OH MEDPRIDE (SODIUM MONOFLUOROPHOSPHATE ) PASTE, DENTIFRICE [SHIELD LINE LLC ] 1 SACCHARIN SODIUM INACTIVE INGREDIENT SB8ZUX40TY MEDPRIDE (SODIUM MONOFLUOROPHOSPHATE ) PASTE, DENTIFRICE [SHIELD LINE LLC ] 1 SODIUM LAURYL SULFATE INACTIVE INGREDIENT 368GB5141J MEDPRIDE (SODIUM MONOFLUOROPHOSPHATE ) PASTE, DENTIFRICE [SHIELD LINE LLC ] 1 SORBITOL INACTIVE INGREDIENT 506T60A25R MEDPRIDE (SODIUM MONOFLUOROPHOSPHATE ) PASTE, DENTIFRICE [SHIELD LINE LLC ] 1 WATER INACTIVE INGREDIENT 059QF0KO0R MEDPRIDE (SODIUM MONOFLUOROPHOSPHATE ) PASTE, DENTIFRICE [SHIELD LINE LLC ] 1
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 52410-9005 MEDPRIDE (SODIUM MONOFLUOROPHOSPHATE) PASTE, DENTIFRICE [SHIELD LINE LLC] 5 Current NDC, Legacy NDC, 2 package rows 20250117_9c1b0420-6b57-4914-99fe-df6a494815c3.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 52410-9005-3 52410900503 42.5 g in 1 TUBE (52410-9005-3) 42.5 g 2013-05-27 0000-00-00 No No Current 52410-9005-4 52410900504 78 g in 1 TUBE (52410-9005-4) 78 g 2013-05-27 0000-00-00 No No Current