Home NDC 10056-415 Glister Multi-Action
Product NDC 10056-415
11-digit product format 100560415
Labeler code 10056
Product ID 10056-415_085bbc1a-0302-ea11-e063-6394a90a3391
Type HUMAN OTC DRUG
Nonproprietary name SODIUM FLUORIDE
Dosage form PASTE, DENTIFRICE
Route DENTAL
Labeler Access Business Group LLC
Application M021
Marketing category OTC MONOGRAPH DRUG
Marketing start 2023-03-22
Substance SODIUM FLUORIDE
Active strength 2.1 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 Glister Multi-Action
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength SODIUM FLUORIDE 2.1 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 1099038 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 10056-415-00 Glister Multi-Action 50 g in 1 TUBE PASTE, DENTIFRICE 50 2 10056-415-00 Glister Multi-Action 1 in 1 CARTON PASTE, DENTIFRICE 1 2 10056-415-01 Glister Multi-Action 1 in 1 CARTON PASTE, DENTIFRICE 1 2 10056-415-01 Glister Multi-Action 200 g in 1 TUBE PASTE, DENTIFRICE 200 2
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 10056-415 GLISTER MULTI-ACTION (SODIUM FLUORIDE) PASTE, DENTIFRICE [ACCESS BUSINESS GROUP LLC] 2 Current NDC, 4 package rows 20231023_e3f2c049-a0f5-4649-a4aa-11bdb252f951.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 40 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 10056-415-00 10056041500 1 TUBE in 1 CARTON (10056-415-00) / 50 g in 1 TUBE 1 tube 2023-03-22 No No Current 10056-415-01 10056041501 1 TUBE in 1 CARTON (10056-415-01) / 200 g in 1 TUBE 1 tube 2023-03-22 No No Current