Home NDC 11822-0613 3X Medicated Toothache and Gum Gel
Product NDC 11822-0613
11-digit product format 118220613
Labeler code 11822
Product ID 11822-0613_47b7b1c8-6965-dd9c-e063-6294a90a6417
Type HUMAN OTC DRUG
Nonproprietary name Benzocaine
Dosage form GEL
Route ORAL
Labeler Rite Aid
Application M017
Marketing category OTC MONOGRAPH DRUG
Marketing start 2020-05-06
Marketing end 2027-11-01
Substance BENZOCAINE; MENTHOL; ZINC CHLORIDE
Active strength 20; .26; .15 g/100g; g/100g; g/100g
Pharmacologic classes Allergens [CS], Cell-mediated Immunity [PE], Copper Absorption Inhibitor [EPC], Decreased Copper Ion Absorption [PE], Increased Histamine Release [PE], Standardized Chemical Allergen [EPC]
NDC exclude flag No
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 · 14 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 2025-04-01 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 11822-0613-9 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 11822-0613-9 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 11822-0613-9 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 11822-0613-9 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 11822-0613-9 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 11822-0613-9 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 11822-0613-9 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 3X Medicated Toothache and Gum Gel Active Ingredients# Ingredient, Strength table Ingredient Strength BENZOCAINE 20 g/100g MENTHOL .26 g/100g ZINC CHLORIDE .15 g/100g
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 3 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination U3RSY48JW5 Internal UNII lookup L7T10EIP3A Internal UNII lookup 86Q357L16B Internal UNII lookup
Harmonized RxCUI identifiers# RxCUI identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 2362013 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# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 11822-0613-9 3X Medicated Toothache and Gum Gel 1 in 1 CARTON GEL 1 5 11822-0613-9 3X Medicated Toothache and Gum Gel 11.7 g in 1 TUBE GEL 11.7 5
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 11822-0613 3X MEDICATED TOOTHACHE AND GUM GEL (BENZOCAINE) GEL [RITE AID] 3 Current NDC, Legacy NDC, 2 package rows 20230115_996f7989-17ce-5b28-e053-2995a90af8b8.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 39 of 152 · 3,029 matching rows.
Brand, Generic, Manufacturer table Brand Generic Manufacturer SPL set ID Effective date Available safety fields Join Easment advanced absorption cream CAPSAICIN 0.1% Easment LLC 48de3ced-f67f-7c86-e063-6294a90a340c 2026-01-20 Warnings Exact identifier application number: M017 Black Cobra Tattoo NumbingSpray 4% Lidocaine LIDOCAINE Foshan Sugar Max Cosmetics CO.,Ltd 3605fcbf-63c8-87b5-e063-6294a90a9c3e 2026-01-19 Warnings Exact identifier application number: M017 Black Cobra Tattoo Numbing Cream 4% Lidocaine LIDOCAINE Foshan Sugar Max Cosmetics CO.,Ltd 3605961a-d596-9c4a-e063-6394a90a99dc 2026-01-19 Warnings Exact identifier application number: M017 Bakers Best Arthritis Pain Relief HISTAMINE DIHYDROCHLORIDE Baker's Best Health Products, LLC 869735f9-335e-4a5e-adfc-91167ae943c5 2026-01-19 Warnings Exact identifier application number: M017 SIMPLY VITAL PAIN RELIEF HEMP MENTHOL ALPHA PLANTS INC c14f4c06-cfe5-497e-9f9e-b2ba442e61bb 2026-01-19 Warnings Exact identifier application number: M017 AsperFlex MENTHOL AND METHYL SALICYLATE Akron Pharma Inc. 117de175-976d-44f3-85ed-3d127fbe3a7c 2026-01-19 Warnings Exact identifier application number: M017 Equate Pain Relieving Ultra Strength CAMPHOR, MENTHOL, METHYL SALICYLATE Wal-Mart Stores Inc 5ed1d7b3-925e-4a18-8e15-636f5b442ad7 2026-01-19 Warnings Exact identifier application number: M017 Equate Medicated Pain Relieving Patch, Large 6-Count CAMPHOR, MENTHOL, METHYL SALICYLATE Walmart Stores Inc 2c25cd7a-7e7b-5add-e063-6294a90a9e9b 2026-01-19 Warnings Exact identifier application number: M017 Equate Hydrocortione 1% HYDROCORTISONE Walmart Inc. 85b7f620-cc95-4333-b124-bbcc8fd5f7eb 2026-01-19 Warnings Exact identifier application number: M017 GuruNanda Pain Relief MENTHOL GURUNANDA, LLC 3f1d146e-0d18-7f2f-e063-6394a90ab816 2026-01-19 Warnings Exact identifier application number: M017 Aspercreme with Lidocaine LIDOCAINE Chattem, Inc. 7ad8efa9-7031-4cd0-be1d-6dee63091fd1 2026-01-19 Warnings Exact identifier application number: M017 Best Choice Targeted Warming Capsaicin Heat Patch CAPSAICIN Valu Merchandisers Company 24ca40b7-e17b-42a3-bcc8-6861b9a5934a 2026-01-18 Warnings Exact identifier application number: M017 TOPCARE PAIN RELIEF PATCHES LIDOCAINE TOPCO ASSOCIATES, LLC fa2f7768-e779-4409-aad3-6c33ce2e6b36 2026-01-18 Warnings Exact identifier application number: M017 Neuropathy Pain Relief Cream MENTHOL CREAM Owell Naturals Brand, LLC 48979093-2992-5fd8-e063-6394a90a815d 2026-01-17 Warnings Exact identifier application number: M017 CVS Lidocaine Pain Relief Cream LIDOCAINE HYDROCHLORIDE CVS Pharmacy 45c4f946-13b9-7a0a-e063-6394a90a7353 2026-01-16 Warnings Exact identifier application number: M017 TopCare Pain Relieving Cream LIDOCAINE HCL 4% Topco Associates, LLC 4885a7e6-a127-450a-e063-6294a90a4f91 2026-01-16 Warnings Exact identifier application number: M017 Calmara CALMARA Dynarex Corporation 487393e9-6619-6033-e063-6294a90a68b2 2026-01-16 Warnings Exact identifier application number: M017 Maximum Strength Hydrocortisone HYDROCORTISONE OINTMENT Walgreens 7088092c-3a5f-4fcc-84cc-931d238f7501 2026-01-15 Warnings Exact identifier application number: M017 Itch Relief Gel DIPHENHYDRAMINE HCL Walgreens 487060a7-dff3-4840-b967-ca919f8d0a29 2026-01-15 Warnings Exact identifier application number: M017 Walgreen Itch Relief Gel DIPHENHYDRAMINE HYDROCHLORIDE Walgreens 5aca3297-406f-4165-9895-c58ccffb374f 2026-01-15 Warnings Exact identifier application number: M017
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 11822-0613-9 11822061309 1 TUBE in 1 CARTON (11822-0613-9) / 11.7 g in 1 TUBE 1 tube 2020-05-06 2027-11-01 No No Current