Home NDC 10129-034-01 GingiCaine Gel, Chocolate Mint
Product NDC 10129-034
Requested package NDC 10129-034-01
11-digit product format 101290034
Labeler code 10129
Product ID 10129-034_d2bb20bd-ec82-8d80-e053-2a95a90a2bba
Type HUMAN OTC DRUG
Nonproprietary name GingiCaine Gel, Chocolate Mint Flavor
Dosage form GEL
Route DENTAL; ORAL; PERIODONTAL
Labeler Gingi-Pak a Division of the Belport
Application part356
Marketing category OTC MONOGRAPH NOT FINAL
Marketing start 1993-07-06
Marketing end 0000-00-00
Substance BENZOCAINE
Active strength 200 mg/1
Pharmacologic classes Allergens [CS]; Cell-mediated Immunity [PE]; Increased Histamine Release [PE]; Standardized Chemical Allergen [EPC]
NDC exclude flag No
Listing certified through 2022-12-31
Current FDA listing Historical FDA.report record Observed NDC auxiliary status history# This history shows the information present in each captured FDA auxiliary file. It is not a continuous regulatory timeline, and a missing record does not establish a status.
Historic NDC status page 1 of 1 · 9 matching rows.
View current auxiliary records. · View the auxiliary file history.
Captured / source date, Code, Status table Captured / source date Code Status Snapshot Source SHA-256 2025-12-14 17:58 UTC · source 2025-12-05 I Inactivated by FDA d630ba8d3edf…732f749b63fb…2025-08-27 00:01 UTC · source 2025-08-26 I Inactivated by FDA f5e01cc5f278…a2eaf40c39c3…2025-04-01 02:39 UTC · source 2025-03-31 I Inactivated by FDA 2ef7874e63bc…57b86245f4fa…2025-03-28 20:22 UTC · source 2025-03-28 I Inactivated by FDA a1b67e2a42f9…c4cf2c586c0d…2025-03-22 03:12 UTC · source 2025-03-21 I Inactivated by FDA cfe11265f3b6…090c488252e2…2025-03-10 12:48 UTC · source 2025-03-10 I Inactivated by FDA cdf11ea48f46…ba0047e9e063…2025-02-02 03:52 UTC · source 2025-01-31 U Excluded because listing certification expired 302b2466d912…e7b80fea0513…2025-01-20 13:05 UTC · source 2025-01-20 U Excluded because listing certification expired ed331223b511…672a5bd82f5f…2025-01-11 03:41 UTC · source 2025-01-10 U Excluded because listing certification expired 0efc9e666f02…f202fb6c5f17…
Additional Listing Data#
Finished product Yes
Brand name base GingiCaine Gel, Chocolate Mint
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength BENZOCAINE 200 mg/1
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination U3RSY48JW5 Internal UNII lookup
Harmonized RxCUI identifiers# RxCUI identifiers page 1 of 1 · 2 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 238910 Internal RxNorm lookup 543801 Internal RxNorm lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Product Concepts# FDA-Initiated Inactive NDC Indexing# NDC, Effective, Related label table NDC Effective Related label 10129-034-01 2025-01-30 GingiCaine Gel, Chocolate Mint 10129-034-01 2025-01-30 GingiCaine Gel, Chocolate Mint 10129-034-05 2025-01-30 GingiCaine Gel, Chocolate Mint 10129-034-05 2025-01-30 GingiCaine Gel, Chocolate Mint 10129-034-01 2021-09-02 GingiCaine Gel, Chocolate Mint 10129-034-01 2021-09-02 GingiCaine Gel, Chocolate Mint 10129-034-05 2021-09-02 GingiCaine Gel, Chocolate Mint 10129-034-05 2021-09-02 GingiCaine Gel, Chocolate Mint 10129-034-01 2021-07-23 GingiCaine Gel, Chocolate Mint 10129-034-01 2021-07-23 GingiCaine Gel, Chocolate Mint 10129-034-05 2021-07-23 GingiCaine Gel, Chocolate Mint 10129-034-05 2021-07-23 GingiCaine Gel, Chocolate Mint
DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 10129-034-01 GingiCaine Gel, Chocolate Mint 1 in 1 BOTTLE, PLASTIC GEL 1 2 10129-034-05 GingiCaine Gel, Chocolate Mint 6 in 1 BOTTLE, PLASTIC GEL 6 2
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 10129-034 GINGICAINE GEL, CHOCOLATE MINT (GINGICAINE GEL, CHOCOLATE MINT FLAVOR) GEL [GINGI-PAK A DIVISION OF THE BELPORT] 2 Legacy NDC, 2 package rows 20211210_6285c4f2-c139-49a9-e053-2991aa0a2b03.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.
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 10129-034-01 10129003401 1 GEL in 1 BOTTLE, PLASTIC (10129-034-01) 1 gel 1993-07-06 0000-00-00 No No Current