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 2 of 41 · 818 matching rows.
Brand, Generic, Manufacturer table Brand Generic Manufacturer SPL set ID Effective date Available safety fields Join Ludens Watermelon Throat Drops PECTIN Prestige Brands Holdings, Inc. adfb248a-96bb-4742-9df6-c47edccdd671 2026-08-20 Warnings Exact identifier application number: M022 Antiseptic EUCALYPTOL, MENTHOL, METHYL SALICYLATE, THYMOL WALMART INC. (see also Equate) 584b38ce-d1ef-4ecc-a887-7c96e7f9669f 2026-08-20 Warnings Exact identifier application number: M022 Antiseptic EUCALYPTOL, MENTHOL, METHYL SALICYLATE, THYMOL Walgreens fb93c7f6-e025-4cf2-9997-acfe9a0debdd 2026-08-19 Warnings Exact identifier application number: M022 CVS Saline NASAL CVS PHARMACY f02c41b0-c78e-41cd-aa4a-2756bbe92087 2026-08-19 Warnings Exact identifier application number: M022 Listerine UltraClean Gum Plus Whitening Protection Cool Mint Antigingivitis/ Antiplaque Mouthwash EUCALYPTOL, MENTHOL, METHYL SALICYLATE, THYMOL Kenvue Brands LLC 5965eb2a-1261-5258-e063-6294a90a7c2d 2026-08-19 Warnings Exact identifier application number: M022 Ludens Honey Licorice Throat Drops MENTHOL Prestige Brands Holdings, Inc. 5dc2baec-a9ed-4f6b-a7ed-76a5d35739ac 2026-08-19 Warnings Exact identifier application number: M022 Ludens Dual Relief PECTIN AND MENTHOL Prestige Brands Holdings, Inc. d0213cb3-ec8e-40cc-82c9-694032f0490f 2026-08-19 Warnings Exact identifier application number: M022 CVS Health Sore Throat Fast Relief Oral Anesthetic PHENOL CVS Pharmacy,Inc. 4fb880db-2185-41ef-a5f9-8983a28d2c5b 2026-08-17 Warnings Exact identifier application number: M022 CVS Sore Throat Cherry PHENOL CVS Pharmacy,Inc. 887c68e0-ff44-4bad-b360-56fb99ed9c45 2026-08-17 Warnings Exact identifier application number: M022 CVS Sore Throat Menthol Flavor PHENOL CVS PHARMACY,INC. 665be058-b965-4b78-80b0-dd8524180932 2026-08-17 Warnings Exact identifier application number: M022 Hydrogen Peroxide 3 Percent HYDROGEN PEROXIDE Harris Teeter, LLC 7e5f175d-f0d6-4665-ac14-1873d6b99c80 2026-08-12 Warnings Exact identifier application number: M022 Gingicaine Gel Variety Pak GINGICAINE GEL VARIETY PAK Gingi-Pak a Division of the Belport 62ed4ff3-18f6-5c67-e053-2991aa0a7792 2026-08-11 Warnings Exact identifier application number: M022 Hydrogen Peroxide 3 Percent ReadyInCase HYDROGEN PEROXIDE P & L Development, LLC b0866db5-3b0d-4478-9b3b-1f077d2f5393 2026-08-06 Warnings Exact identifier application number: M022 Ollie Fresh Mint SODIUM FLUORIDE, POTASSIUM NITRATE Brio Product Group LLC. ebeec44f-3c22-43f2-9256-6ece6025c105 2026-08-06 Warnings Exact identifier application number: M022 Candee Caine Topical Anesthetic BENZOCAINE Top Quality Manufacturing, Inc. 5868c5a1-273f-f023-e063-6394a90ac9d8 2026-08-06 Warnings Exact identifier application number: M022 Candee Caine Topical Anesthetic BENZOCAINE Top Quality Manufacturing, Inc. 58690bb5-9604-26a4-e063-6394a90afdbe 2026-08-06 Warnings Exact identifier application number: M022 Candee Caine Topical Anesthetic BENZOCAINE Top Quality Manufacturing, Inc. 586918cf-7b13-5999-e063-6294a90a88a9 2026-08-06 Warnings Exact identifier application number: M022 Candee Caine Topical Anesthetic BENZOCAINE Top Quality Manufacturing, Inc. 586924a0-322d-5dc3-e063-6294a90a1556 2026-08-06 Warnings Exact identifier application number: M022 Candee Caine Topical Anesthetic BENZOCAINE Top Quality Manufacturing, Inc. 58692e90-de74-52d3-e063-6394a90a9702 2026-08-06 Warnings Exact identifier application number: M022 Candee Caine Topical Anesthetic BENZOCAINE Top Quality Manufacturing, Inc. 586937ae-46af-7066-e063-6294a90ae53e 2026-08-06 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