Home NDC 73242-1120 DENTI BUONGIORNO ORIGINAL TOOTH
Product NDC 73242-1120
11-digit product format 732421120
Labeler code 73242
Product ID 73242-1120_4119a974-5d1d-c809-e063-6294a90a635d
Type HUMAN OTC DRUG
Nonproprietary name Silica, Sodium Monofluorophosphate
Dosage form PASTE, DENTIFRICE
Route ORAL
Labeler DONG IL PHARMS CO.,LTD
Marketing category UNAPPROVED DRUG OTHER
Marketing start 2025-04-01
Substance SILICON DIOXIDE; SODIUM MONOFLUOROPHOSPHATE
Active strength 18; .76 g/100g; g/100g
NDC exclude flag No
Listing certified through 2026-12-31
Current FDA listing Yes Additional Listing Data#
Finished product Yes
Brand name base DENTI BUONGIORNO ORIGINAL TOOTH
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength SILICON DIOXIDE 18 g/100g SODIUM MONOFLUOROPHOSPHATE .76 g/100g
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 2 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination ETJ7Z6XBU4 Internal UNII lookup C810JCZ56Q Internal UNII 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 73242-1120-1 DENTI BUONGIORNO ORIGINAL TOOTH 100 g in 1 TUBE PASTE, DENTIFRICE 100 1 73242-1120-2 DENTI BUONGIORNO ORIGINAL TOOTH 1 in 1 CARTON 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 1 of 1 · 1 matching rows.
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Sample Exclude flag Status 73242-1120-1 73242112001 100 g in 1 TUBE 100 g Historical 73242-1120-2 73242112002 1 TUBE in 1 CARTON (73242-1120-2) / 100 g in 1 TUBE (73242-1120-1) 1 tube 2025-04-01 No No Current