Home NDC 35000-900 COLGATE SPARKLING WHITE CINNAMINT
Product NDC 35000-900
11-digit product format 350000900
Labeler code 35000
Product ID 35000-900_a398e1b8-85e2-4f49-8f36-00e6bd9d6659
Type HUMAN OTC DRUG
Nonproprietary name SODIUM FLUORIDE
Dosage form GEL, DENTIFRICE
Route DENTAL
Labeler Colgate-Palmolive Company
Application M021
Marketing category OTC MONOGRAPH DRUG
Marketing start 2012-10-01
Substance SODIUM FLUORIDE
Active strength 1.1 mg/g
NDC exclude flag No
Listing certified through 2027-12-31
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 · 10 matching rows.
View current auxiliary records. · View the auxiliary file history.
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 COLGATE SPARKLING WHITE CINNAMINT
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength SODIUM FLUORIDE 1.1 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 416783 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 35000-900-60 COLGATE SPARKLING WHITE CINNAMINT 170 g in 1 TUBE GEL, DENTIFRICE 170 5 35000-900-60 COLGATE SPARKLING WHITE CINNAMINT 1 in 1 CARTON GEL, DENTIFRICE 1 5 35000-900-64 COLGATE SPARKLING WHITE CINNAMINT 1 in 1 CARTON GEL, DENTIFRICE 1 5 35000-900-64 COLGATE SPARKLING WHITE CINNAMINT 181 g in 1 TUBE GEL, DENTIFRICE 181 5 35000-900-69 COLGATE SPARKLING WHITE CINNAMINT 1 in 1 CARTON GEL, DENTIFRICE 1 5 35000-900-69 COLGATE SPARKLING WHITE CINNAMINT 113 g in 1 TUBE GEL, DENTIFRICE 113 5
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 35000-900 COLGATE SPARKLING WHITE CINNAMINT (SODIUM FLUORIDE) GEL, DENTIFRICE [COLGATE PALMOLIVE COMPANY] 3 Current NDC, Legacy NDC, 6 package rows 20241127_f2ff18d2-4ef0-454e-a6f1-6f3bf361c7d1.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 7 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 35000-900-60 35000090060 1 TUBE in 1 CARTON (35000-900-60) > 170 g in 1 TUBE 1 tube 2012-10-01 0000-00-00 No No Current 35000-900-64 35000090064 1 TUBE in 1 CARTON (35000-900-64) > 181 g in 1 TUBE 1 tube 2012-10-01 0000-00-00 No No Current 35000-900-69 35000090069 1 TUBE in 1 CARTON (35000-900-69) / 113 g in 1 TUBE 1 tube 2012-10-01 0000-00-00 No No Current