Home NDC 10129-062 Gingi-Aid MAX Z-Twist 3
Product NDC 10129-062
11-digit product format 101290062
Labeler code 10129
Product ID 10129-062_638dbc25-481e-3d56-e053-2a91aa0a9554
Type HUMAN OTC DRUG
Nonproprietary name Gingi-Aid MAX Z-Twist 3
Dosage form SOLUTION
Route DENTAL; ORAL; PERIODONTAL; SUBGINGIVAL
Labeler Gingi-Pak a Division of the Belport
Application part347
Marketing category OTC MONOGRAPH FINAL
Marketing start 1998-07-31
Marketing end 0000-00-00
Substance ALUMINUM SULFATE
Active strength 54 mg/1
NDC exclude flag No
Listing certified through 2020-12-31
Current FDA listing Historical FDA.report record FDA-Initiated Inactive NDC Indexing# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 10129-062-03 Gingi-Aid MAX Z-Twist 3 1 in 1 VIAL, PLASTIC SOLUTION 1 1
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 10129-062 GINGI-AID MAX Z-TWIST 1 SOLUTION GINGI-AID MAX Z-TWIST 00 SOLUTION GINGI-AID MAX Z-TWIST 3 SOLUTION GINGI-AID MAX Z-TWIST 2 SOLUTION [GINGI-PAK A DIVISION OF THE BELPORT] 1 Legacy NDC, 1 package rows 20180201_638dbc25-481d-3d56-e053-2a91aa0a9554.zip
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 10129-062-03 10129006203 1 SOLUTION in 1 VIAL, PLASTIC (10129-062-03) 1 solution 1998-07-31 0000-00-00 No No Current