Home NDC 73527-0004-1 MIMIBO PREMIUM TOOTH
Product NDC 73527-0004
Requested package NDC 73527-0004-1
11-digit product format 735270004
Labeler code 73527
Product ID 73527-0004_2ac515e8-9acc-e60f-e063-6394a90af897
Type HUMAN OTC DRUG
Nonproprietary name Silicon Dioxide, Tocopherol Acetate, Tetrasodium Pyrophosphate
Dosage form PASTE, DENTIFRICE
Route DENTAL
Labeler CONE MEDICAL Co., Ltd.
Marketing category UNAPPROVED DRUG OTHER
Marketing start 2021-04-01
Substance .ALPHA.-TOCOPHEROL ACETATE; SILICON DIOXIDE; SODIUM PYROPHOSPHATE
Active strength .1; 14; .5 g/100g; 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 MIMIBO PREMIUM TOOTH
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength SILICON DIOXIDE .1 g/100g .ALPHA.-TOCOPHEROL ACETATE 14 g/100g SODIUM PYROPHOSPHATE .5 g/100g
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 3 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination ETJ7Z6XBU4 Internal UNII lookup 9E8X80D2L0 Internal UNII lookup O352864B8Z Internal UNII lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
FDA-Initiated Inactive NDC Indexing# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 73527-0004-1 MIMIBO PREMIUM TOOTH 20 g in 1 TUBE PASTE, DENTIFRICE 20 4
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 73527-0004 MIMIBO PREMIUM TOOTH (SILICON DIOXIDE, TOCOPHEROL ACETATE, TETRASODIUM PYROPHOSPHATE) PASTE, DENTIFRICE [CONE MEDICAL CO., LTD.] 4 Current NDC, Legacy NDC, 1 package rows 20250104_c101881a-5a12-2e04-e053-2a95a90a3f57.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 1 of 1 · 1 matching rows.
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 73527-0004-1 73527000401 20 g in 1 TUBE (73527-0004-1) 20 g 2021-04-01 0000-00-00 No No Current