Home NDC 61596-802 MIPaste Plus Vanilla
Product NDC 61596-802
11-digit product format 615960802
Labeler code 61596
Product ID 61596-802_4651aba1-945a-d900-e063-6394a90a493a
Type HUMAN OTC DRUG
Nonproprietary name MIPaste Plus Vanilla
Dosage form PASTE, DENTIFRICE
Route DENTAL
Labeler GC America Inc.
Application M021
Marketing category OTC MONOGRAPH DRUG
Marketing start 2022-02-03
Substance SODIUM FLUORIDE
Active strength .2 g/100g
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 MIPaste Plus Vanilla
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength SODIUM FLUORIDE .2 g/100g
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 1235783 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 61596-802-10 MIPaste Plus Vanilla 10 in 1 BOX PASTE, DENTIFRICE 10 3 61596-802-40 MIPaste Plus Vanilla 40 g in 1 TUBE PASTE, DENTIFRICE 40 3 61596-802-41 MIPaste Plus Vanilla 1 in 1 BOX, UNIT-DOSE PASTE, DENTIFRICE 1 3
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 61596-802 MIPASTE PLUS VANILLA PASTE, DENTIFRICE [GC AMERICA INC.] 2 Current NDC, Legacy NDC, 3 package rows 20240128_d7244125-1ca5-78ba-e053-2995a90ab764.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 51 · 1,013 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 61596-802-10 61596080210 10 BOX, UNIT-DOSE in 1 BOX (61596-802-10) / 1 TUBE in 1 BOX, UNIT-DOSE (61596-802-41) / 40 g in 1 TUBE (61596-802-40) 2022-02-03 0000-00-00 No No Current 61596-802-40 61596080240 40 g in 1 TUBE 40 g Historical 61596-802-41 61596080241 1 in 1 BOX, UNIT-DOSE Historical