Home NDC 27017-142 Spry Dentifrice
Product NDC 27017-142
11-digit product format 270170142
Labeler code 27017
Product ID 27017-142_43567bbc-b07f-b605-e063-6294a90aad78
Type HUMAN OTC DRUG
Nonproprietary name Toothpaste
Dosage form PASTE, DENTIFRICE
Route ORAL
Labeler Xlear Inc.
Application M021
Marketing category OTC MONOGRAPH DRUG
Marketing start 2017-06-11
Substance SODIUM FLUORIDE
Active strength 2.43 mg/g
NDC exclude flag No
Listing certified through 2026-12-31
Current FDA listing Yes 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 Spry Dentifrice
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength SODIUM FLUORIDE 2.43 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.
DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 27017-142-01 Spry Dentifrice 1 g in 1 TUBE PASTE, DENTIFRICE 1 1
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 Sample Exclude flag Status 27017-142-01 27017014201 1 g in 1 TUBE (27017-142-01) 1 g 2017-06-11 No No Current