Home NDC 71888-101 Benzocaine
Product NDC 71888-101
11-digit product format 718880101
Labeler code 71888
Product ID 71888-101_47fac2e8-50dd-cddf-e063-6394a90a9176
Type HUMAN OTC DRUG
Nonproprietary name Benzocaine
Dosage form GEL
Route TOPICAL
Labeler Bellus Medical, LLC
Application M017
Marketing category OTC MONOGRAPH DRUG
Marketing start 2017-06-01
Substance BENZOCAINE
Active strength 200 mg/mL
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 · 12 matching rows.
View current auxiliary records. · View the auxiliary file history.
Captured / source date, Dataset, Scope table Captured / source date Dataset Scope Package NDC Snapshot Source SHA-256 2022-08-30 03:57 UTC · source 2022-08-29 excluded product product fb8cb913e6d1…eb8c232b6be0…2022-08-30 03:57 UTC · source 2022-08-29 excluded package package 71888-101-02 fb8cb913e6d1…eb8c232b6be0…2022-04-09 23:13 UTC · source 2022-04-08 excluded product product 86f5da6cb304…a595104c45d7…2022-04-09 23:13 UTC · source 2022-04-08 excluded package package 71888-101-02 86f5da6cb304…a595104c45d7…2022-04-04 05:40 UTC · source 2022-04-01 excluded product product bd6a592717d7…303034d00443…2022-04-04 05:40 UTC · source 2022-04-01 excluded package package 71888-101-02 bd6a592717d7…303034d00443…2021-12-27 23:28 UTC · source 2021-12-27 excluded product product 8dfbde2a14a4…c9ff85d89658…2021-12-27 23:28 UTC · source 2021-12-27 excluded package package 71888-101-02 8dfbde2a14a4…c9ff85d89658…2020-12-18 03:04 UTC · source 2020-12-17 excluded product product e2bbac7714bc…27bdfed8d636…2020-12-18 03:04 UTC · source 2020-12-17 excluded package package 71888-101-02 e2bbac7714bc…27bdfed8d636…2020-06-10 20:45 UTC · source 2020-06-10 excluded product product 9bebd1f3094a…5416666fcb17…2020-06-10 20:45 UTC · source 2020-06-10 excluded package package 71888-101-02 9bebd1f3094a…5416666fcb17…
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 Benzocaine
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength BENZOCAINE 200 mg/mL
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 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 452688 Internal RxNorm lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
FDA-Initiated Inactive NDC Indexing# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 71888-101-01 Benzocaine 4 mL in 1 PACKET GEL 4 4 71888-101-02 Benzocaine 12 in 1 BOX GEL 12 4
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 71888-101 BENZOCAINE GEL [BELLUS MEDICAL, LLC] 3 Current NDC, Legacy NDC, 2 package rows 20241120_60cafbaf-8ec6-46a5-e053-2a91aa0af11f.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 33 of 153 · 3,057 matching rows.
Brand, Generic, Manufacturer table Brand Generic Manufacturer SPL set ID Effective date Available safety fields Join Tylenol Precise Cooling Pain Relieving LIDOCAINE, MENTHOL Kenvue Brands LLC fc0a3404-b174-3952-e053-6294a90a1e02 2026-02-16 Warnings Exact identifier application number: M017 Aloe Vera Gel LIDOCAINE HCL Valu Merchandisers Company 87ee2b4f-d640-4cec-9f48-1d8aa54434e9 2026-02-16 Warnings, Adverse reactions Exact identifier application number: M017 Hemp Magic Fast-Acting Pain Relief Cream MENTHOL Nexxus Capital LLC 4af69640-1413-868b-e063-6394a90a3989 2026-02-16 Warnings Exact identifier application number: M017 RelaxInk LIDOCAINE LIDOCAINE 4% Hambli Limited 49a1cf66-9bb1-b918-e063-6394a90a2ff6 2026-02-15 Warnings Exact identifier application number: M017 blue goo Pain Relieving MENTHOL 2.5% Garcoa, Inc. 7b9b5ac6-9568-464c-8096-0302a1e650df 2026-02-13 Warnings Exact identifier application number: M017 Methyl Salicylate 30 Percent Cream METHYL SALICYLATE Alexso, Inc 1d50ccb2-1a5d-49c7-8524-2f54eed63e85 2026-02-13 Warnings Exact identifier application number: M017 Antiseptic Mouth Rinse EUCALYPTOL, MENTHOL, METHYOL SALICYLATE, THYMOL Topco Associates LLC a38e91c1-7ac6-4a7f-a5a2-8d9166b1535a 2026-02-13 Warnings, Adverse reactions Exact identifier application number: M017 Gel Cooling Pain Relief MENTHOL Topco Associates LLC 80962394-a46f-48fd-8e0c-685dd1e500d7 2026-02-13 Warnings, Adverse reactions Exact identifier application number: M017 Banophen DIPHENHYDRAMINE HYDROCHLORIDE, ZINC ACETATE Major Pharmaceuticals 9758d886-bd58-4eb2-a827-fa8e7fee2b7c 2026-02-13 Warnings Exact identifier application number: M017 Natureplex Hydrocortisone Hydro HYDROCORTISONE Natureplex, LLC 2fc6a148-34bb-4289-8588-32c1bb011b98 2026-02-13 Warnings Exact identifier application number: M017 Capsaicin 0.035 Percent CAPSAICIN Alexso, Inc 6d0bc1cc-e812-4753-b20c-c0357dd6deb5 2026-02-13 Warnings Exact identifier application number: M017 Swiftalyn Numbing Cream LIDOCAINE 4% GENUINE INNOVATION LTD 3f74c4a6-26f0-ddf7-e063-6394a90a1225 2026-02-12 Warnings Exact identifier application number: M017 PHARMBANNER Arnica Bruise Cream ARNICA BRUISE CREAM Shenzhen Xinxin Yunhai Technology Co., Ltd. 3c783061-8e2d-8a84-e063-6394a90a5265 2026-02-12 Warnings Exact identifier application number: M017 ETERNAL SPIRIT BEAUTY PAIN RELIEF WITH HEMP MENTHOL, CAMPHOR Worldwide Cosmetics, Inc 459d64a9-0538-57c8-e063-6394a90a6155 2026-02-12 Warnings Exact identifier application number: M017 Antiseptic Mouth Rinse EUCALYPTOL Walgreen Co. cba60e9d-5f12-4c56-9fa5-6ce1514fc2b0 2026-02-12 Warnings, Adverse reactions Exact identifier application number: M017 Medicated Body Powder MENTHOL Walmart Stores Inc afd337b7-d76e-f17a-e053-2a95a90abac7 2026-02-12 Warnings Exact identifier application number: M017 Lidocaine Hydrochloride 2% LIDOCAINE HYDROCHLORIDE Aldermed Inc. 4977b722-d08d-3d9e-e063-6294a90a9035 2026-02-12 Warnings Exact identifier application number: M017 Ice Gel ICE COLD ANALGESIC MENTHOL Jell Pharmaceuticals Pvt Ltd 4a8b3f84-8c45-eb94-e063-6394a90a3e73 2026-02-11 Warnings Exact identifier application number: M017 Walgreens Pain Relieving Lidocaine Patch LIDOCAINE Walgreen Co. 41c4e9fe-e407-b22a-e063-6394a90a4b27 2026-02-10 Warnings Exact identifier application number: M017 Hydrocortisone HYDROCORTISONE CREAM 1% Aldermed Inc. 4a7f2c0e-5cf3-29cb-e063-6394a90a5d8d 2026-02-10 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 Sample Exclude flag Status 71888-101-01 71888010101 4 mL in 1 PACKET 4 ml Historical 71888-101-02 71888010102 12 PACKET in 1 BOX (71888-101-02) / 4 mL in 1 PACKET (71888-101-01) 12 packet 2017-06-01 No No Current