Home NDC 10129-034 GingiCaine Gel, Chocolate Mint
Product NDC 10129-034
11-digit product format 101290034
Labeler code 10129
Product ID 10129-034_556cb4b1-8f13-33c6-e063-6294a90a6892
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 M022
Marketing category OTC MONOGRAPH DRUG
Marketing start 1993-07-06
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 2027-12-31
Current FDA listing Yes 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 · 27 matching rows.
View current auxiliary records. · View the auxiliary file history.
Captured / source date, Dataset, Scope table Captured / source date Dataset Scope Package NDC Code Status Snapshot Source SHA-256 2025-12-14 17:58 UTC · source 2025-12-05 excluded product product I Inactivated by FDA d630ba8d3edf…732f749b63fb…2025-12-14 17:58 UTC · source 2025-12-05 excluded package package 10129-034-01 I Inactivated by FDA d630ba8d3edf…732f749b63fb…2025-12-14 17:58 UTC · source 2025-12-05 excluded package package 10129-034-05 I Inactivated by FDA d630ba8d3edf…732f749b63fb…2025-08-27 00:01 UTC · source 2025-08-26 excluded product product I Inactivated by FDA f5e01cc5f278…a2eaf40c39c3…2025-08-27 00:01 UTC · source 2025-08-26 excluded package package 10129-034-01 I Inactivated by FDA f5e01cc5f278…a2eaf40c39c3…2025-08-27 00:01 UTC · source 2025-08-26 excluded package package 10129-034-05 I Inactivated by FDA f5e01cc5f278…a2eaf40c39c3…2025-04-01 02:39 UTC · source 2025-03-31 excluded product product I Inactivated by FDA 2ef7874e63bc…57b86245f4fa…2025-04-01 02:39 UTC · source 2025-03-31 excluded package package 10129-034-01 I Inactivated by FDA 2ef7874e63bc…57b86245f4fa…2025-04-01 02:39 UTC · source 2025-03-31 excluded package package 10129-034-05 I Inactivated by FDA 2ef7874e63bc…57b86245f4fa…2025-03-28 20:22 UTC · source 2025-03-28 excluded product product I Inactivated by FDA a1b67e2a42f9…c4cf2c586c0d…2025-03-28 20:22 UTC · source 2025-03-28 excluded package package 10129-034-01 I Inactivated by FDA a1b67e2a42f9…c4cf2c586c0d…2025-03-28 20:22 UTC · source 2025-03-28 excluded package package 10129-034-05 I Inactivated by FDA a1b67e2a42f9…c4cf2c586c0d…2025-03-22 03:12 UTC · source 2025-03-21 excluded product product I Inactivated by FDA cfe11265f3b6…090c488252e2…2025-03-22 03:12 UTC · source 2025-03-21 excluded package package 10129-034-01 I Inactivated by FDA cfe11265f3b6…090c488252e2…2025-03-22 03:12 UTC · source 2025-03-21 excluded package package 10129-034-05 I Inactivated by FDA cfe11265f3b6…090c488252e2…2025-03-10 12:48 UTC · source 2025-03-10 excluded product product I Inactivated by FDA cdf11ea48f46…ba0047e9e063…2025-03-10 12:48 UTC · source 2025-03-10 excluded package package 10129-034-01 I Inactivated by FDA cdf11ea48f46…ba0047e9e063…2025-03-10 12:48 UTC · source 2025-03-10 excluded package package 10129-034-05 I Inactivated by FDA cdf11ea48f46…ba0047e9e063…2025-02-02 03:52 UTC · source 2025-01-31 excluded product product U Excluded because listing certification expired 302b2466d912…e7b80fea0513…2025-02-02 03:52 UTC · source 2025-01-31 excluded package package 10129-034-01 U Excluded because listing certification expired 302b2466d912…e7b80fea0513…2025-02-02 03:52 UTC · source 2025-01-31 excluded package package 10129-034-05 U Excluded because listing certification expired 302b2466d912…e7b80fea0513…2025-01-20 13:05 UTC · source 2025-01-20 excluded product product U Excluded because listing certification expired ed331223b511…672a5bd82f5f…2025-01-20 13:05 UTC · source 2025-01-20 excluded package package 10129-034-01 U Excluded because listing certification expired ed331223b511…672a5bd82f5f…2025-01-20 13:05 UTC · source 2025-01-20 excluded package package 10129-034-05 U Excluded because listing certification expired ed331223b511…672a5bd82f5f…2025-01-11 03:41 UTC · source 2025-01-10 excluded product product U Excluded because listing certification expired 0efc9e666f02…f202fb6c5f17…2025-01-11 03:41 UTC · source 2025-01-10 excluded package package 10129-034-01 U Excluded because listing certification expired 0efc9e666f02…f202fb6c5f17…2025-01-11 03:41 UTC · source 2025-01-10 excluded package package 10129-034-05 U Excluded because listing certification expired 0efc9e666f02…f202fb6c5f17…
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 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 Current NDC, 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 17 of 41 · 818 matching rows.
Brand, Generic, Manufacturer table Brand Generic Manufacturer SPL set ID Effective date Available safety fields Join Oral Pain Relief BENZOCAINE AND BENZALKONIUM CHLORIDE Universal Distribution Center LLC 18520f9b-4d35-1e9c-e063-6294a90aaa39 2025-10-30 Warnings Exact identifier application number: M022 Iodent Oral Analgesic BENZOCAINE United Exchange Corp. 63902125-f8dc-0ada-e053-2991aa0a7ce5 2025-10-30 Warnings Exact identifier application number: M022 Ear Wax Removal Aid Drops CARBAMIDE PEROXIDE BETTER LIVING BRANDS, LLC 3bded237-4d2c-4b38-bedc-267fdc374194 2025-10-29 Warnings Exact identifier application number: M022 WALMART SALINE SALINE NASAL (SODIUM CHLORIDE) WALMART STORES INC 06906744-49a5-4bab-8539-af2d235df9e8 2025-10-28 Warnings Exact identifier application number: M022 Saline NASAL PUBLIX SUPER MARKETS, INC 19841567-9511-43d6-ba4e-d1e1bd3481a4 2025-10-28 Warnings Exact identifier application number: M022 PUBLIX Sore Throat Fast Relief Oral Anesthetic PHENOL PUBLIX SUPER MARKETS, INC 89291f12-bbc3-4472-8ad3-a34485af72c9 2025-10-28 Warnings Exact identifier application number: M022 PUBLIX Sore Throat Menthol Flavor PHENOL PUBLIX SUPER MARKETS, INC 9296c49e-557c-43ed-9527-fcba5093a8dc 2025-10-28 Warnings Exact identifier application number: M022 WinCo Foods Maximum Strength Oral Analgesic BENZOCAINE WinCo Foods, LLC c22a7726-8c3f-41bf-b852-8456b2be6f93 2025-10-28 Warnings Exact identifier application number: M022 Rugby Cherry Flavor PHENOL RUGBY LABORATORIES 3d668c78-8130-45d4-bcb7-dddcb2fbe7a3 2025-10-25 Warnings Exact identifier application number: M022 LolliCaine Bubble Gum BENZOCAINE Centrix, Inc. 56ae3a84-6bca-4906-a03d-9d755e1fba3b 2025-10-24 Warnings Exact identifier application number: M022 Meijer Sore Throat PHENOL MEIJER DISTRIBUTION INC. 360f9756-1cd7-41b2-8ee2-9d1bb7234cf1 2025-10-24 Warnings Exact identifier application number: M022 MEIJER Saline NASAL MEIJER a5c6d800-078a-4b66-9d4c-cf3c53f5c138 2025-10-24 Warnings Exact identifier application number: M022 meijer Maximum Strength Sore Throat Fast Relief PHENOL AND GLYCERIN MEIJER DISTRIBUTION INC f1f17aab-7ea7-4dac-a854-48b4b560ec4f 2025-10-24 Warnings Exact identifier application number: M022 Diabetic Tussin Sore Throat Cherry PHENOL MEDTECH PRODUCTS INC ab351229-5771-4c6c-92a8-721cc41c002f 2025-10-23 Warnings Exact identifier application number: M022 Chloraseptic Total Sore Throat and Cough, Sugar Free MENTHOL AND BENZOCAINE AND DEXTROMETHORPHAN HYDROBROMIDE Prestige Brands Holdings, Inc. 34e4234c-ed61-4795-99fe-d281cdb0af88 2025-10-23 Warnings Exact identifier application number: M022 Chloraseptic Total Sore Throat and Cough MENTHOL AND BENZOCAINE AND DEXTROMETHORPHAN HYDROBROMIDE Prestige Brands Holdings, Inc. 6b1a50d0-be54-4fcb-b5e2-b47abf3555c0 2025-10-23 Warnings Exact identifier application number: M022 Chloraseptic Childrens Sore Throat Cherry PHENOL Prestige Brands Holdings, Inc. 38ff6922-1abe-4fa9-a74e-ede604f707b5 2025-10-23 Warnings Exact identifier application number: M022 Boka Sensitive POTASSIUM NITRATE Karaka LLC 40be9fab-53db-c67a-e063-6394a90a48cb 2025-10-23 Warnings Exact identifier application number: M022 Canker Care Plus MENTHOL, UNSPECIFIED FORM Quantum, Inc. 1ec960db-52d5-4d99-a7f7-a2e538d28724 2025-10-20 Warnings Exact identifier application number: M022 meijer Sensitive EXTRA WHITENING POTASSIUM NITRATE, SODIUM FLUORIDE Meijer, Inc. bbcffb88-0bd4-4883-bb83-0b7a1428ad12 2025-10-20 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 10129-034-01 10129003401 1 GEL in 1 BOTTLE, PLASTIC (10129-034-01) 1 gel 1993-07-06 0000-00-00 No No Current 10129-034-05 10129003405 6 GEL in 1 BOTTLE, PLASTIC (10129-034-05) 6 gel 1993-07-06 0000-00-00 No No Current