Home NDC 63736-567 Sucrets
Product NDC 63736-567
11-digit product format 637360567
Labeler code 63736
Product ID 63736-567_99b583e8-913d-477d-b658-ea1394d8ddf5
Type HUMAN OTC DRUG
Nonproprietary name Dyclonine HCl, Menthol, and Pectin
Dosage form LOZENGE
Route ORAL
Labeler Insight Pharmaceuticals LLC
Application M022
Marketing category OTC MONOGRAPH DRUG
Marketing start 2014-11-04
Substance DYCLONINE HYDROCHLORIDE; MENTHOL; PECTIN
Active strength 2; 5; 6 mg/1; mg/1; mg/1
NDC exclude flag No
Listing certified through 2027-12-31
Current FDA listing Yes 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 Sucrets
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength DYCLONINE HYDROCHLORIDE 2 mg/1 MENTHOL 5 mg/1 PECTIN 6 mg/1
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 3 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination ZEC193879Q Internal UNII lookup L7T10EIP3A Internal UNII lookup 89NA02M4RX Internal UNII lookup
Harmonized RxCUI identifiers# RxCUI identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 1992531 Internal RxNorm lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Product Concepts# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 63736-567-18 Sucrets 18 in 1 CAN LOZENGE 18 2
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 63736-567 SUCRETS (DYCLONINE HCL, MENTHOL, AND PECTIN) LOZENGE [INSIGHT PHARMACEUTICALS LLC] 2 Current NDC, Legacy NDC, 1 package rows 20240320_2a2839ea-11d3-4390-930d-0da912a9c6f5.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 40 of 40 · 786 matching rows.
Brand, Generic, Manufacturer table Brand Generic Manufacturer SPL set ID Effective date Available safety fields Join Iolite BENZOCAINE Dharma Research, Inc. e4b2d22b-00b3-45a6-9b7d-8ee719587059 2023-10-09 Warnings Exact identifier application number: M022 Iolite BENZOCAINE Dharma Research, Inc. a0e284f6-292f-4231-8596-f7cee4e0a12f 2023-10-09 Warnings Exact identifier application number: M022 HurriCaine Topical Anesthetic BENZOCAINE Beutlich Pharmaceuticals, LLC fe92637a-c88a-f9dd-e053-6294a90a7fa3 2023-07-01 Warnings Exact identifier application number: M022 HurriCaine Topical Anesthetic BENZOCAINE Beutlich Pharmaceuticals, LLC c979e958-2042-471a-bf03-e84e68620106 2023-06-20 Warnings Exact identifier application number: M022 Orajel Gum Pain 3X Medicated BENZOCAINE, MENTHOL, ZINC CHLORIDE Church & Dwight Co., Inc. 9a1632ad-2b47-5653-e053-2995a90ae0d9 2023-01-20 Warnings Exact identifier application number: M022 KOLORZ TOPICAL ANESTHETIC TRIPLE MINT BENZOCAINE DMG AMERICA, LLC 0f90b227-f938-4e1a-a79e-1967b1a0477e 2021-10-01 Warnings Exact identifier application number: M022
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 63736-567-18 63736056718 18 LOZENGE in 1 CAN (63736-567-18) 18 lozenge 2014-11-04 0000-00-00 No No Current