Home NDC 71746-010 YUMAKI ORIGINAL MINT TOOTH
Product NDC 71746-010
11-digit product format 717460010
Labeler code 71746
Product ID 71746-010_fa77277b-e2a2-4a05-a88c-f64c6b54eeda
Type HUMAN OTC DRUG
Nonproprietary name XYLITOL, GREEN TEA LEAF, ASCORBIC ACID, LEVOMENTHOL, PEPPERMINT, AMINOCAPROIC ACID, WATER
Dosage form PASTE, DENTIFRICE
Route TOPICAL
Labeler Jeno And Company
Marketing category UNAPPROVED DRUG OTHER
Marketing start 2017-11-01
Marketing end 0000-00-00
Substance XYLITOL; GREEN TEA LEAF; ASCORBIC ACID; LEVOMENTHOL; PEPPERMINT OIL; AMINOCAPROIC ACID; WATER
Active strength 0 g/100g; g/100g; g/100g; g/100g; g/100g; g/100g; g/100g
NDC exclude flag E
Listing certified through 2018-12-31
Current FDA listing Historical FDA.report record DailyMed Product Concepts# FDA-Initiated Inactive NDC Indexing# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 71746-010-01 YUMAKI ORIGINAL MINT TOOTH 100 g in 1 TUBE PASTE, DENTIFRICE 100 1 71746-010-02 YUMAKI ORIGINAL MINT TOOTH 1 in 1 CARTON PASTE, DENTIFRICE 1 1
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 71746-010 YUMAKI ORIGINAL MINT TOOTH (XYLITOL, GREEN TEA LEAF, ASCORBIC ACID, LEVOMENTHOL, PEPPERMINT, AMINOCAPROIC ACID, WATER) PASTE, DENTIFRICE [JENO AND COMPANY] 1 Legacy NDC, 2 package rows 20171207_e9e39848-2f71-4f32-8bed-b41fc80c5145.zip
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Status 71746-010-01 71746001001 100 g in 1 TUBE 100 g Historical 71746-010-02 71746001002 1 in 1 CARTON Historical