Home NDC 69396-023 Dibucaine
Product NDC 69396-023
11-digit product format 693960023
Labeler code 69396
Product ID 69396-023_0df7b6dd-a4d8-c9a6-e063-6394a90a0f52
Type HUMAN OTC DRUG
Nonproprietary name Dibucaine 1%
Dosage form OINTMENT
Route TOPICAL
Labeler Trifecta Pharmaceuticals USA LLC
Application M017
Marketing category OTC MONOGRAPH DRUG
Marketing start 2022-09-14
Substance DIBUCAINE
Active strength 1 g/100g
Pharmacologic classes Allergens [CS], Cell-mediated Immunity [PE], Increased Histamine Release [PE], Standardized Chemical Allergen [EPC]
NDC exclude flag No
Listing certified through 2026-12-31
Current FDA listing Yes 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 Dibucaine
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength DIBUCAINE 1 g/100g
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination L6JW2TJG99 Internal UNII lookup
Harmonized RxCUI identifiers# RxCUI identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 238784 Internal RxNorm lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 69396-023-01 Dibucaine 28.4 g in 1 TUBE OINTMENT 28.4 2 69396-023-01 Dibucaine 1 in 1 BOX OINTMENT 1 2
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 69396-023 DIBUCAINE (DIBUCAINE 1%) OINTMENT [TRIFECTA PHARMACEUTICALS USA LLC] 2 Current NDC, Legacy NDC, 2 package rows 20240103_e8a56651-a292-7609-e053-2a95a90a7c36.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 12 of 153 · 3,057 matching rows.
Brand, Generic, Manufacturer table Brand Generic Manufacturer SPL set ID Effective date Available safety fields Join Natures Willow Balm Roll On Pain Relief MENTHOL WB Ventures LLC 3b1834e6-75cd-5380-e063-6294a90ad1d5 2026-07-08 Warnings Exact identifier application number: M017 Natures Willow Balm Itch Relief Cream MENTHOL WB Ventures LLC 0ce31b5d-4401-460c-e063-6394a90ab558 2026-07-08 Warnings Exact identifier application number: M017 CAREALL Hydrocortisone Maximum Strength HYDROCORTISONE New World Imports, Inc. 560a4abf-31dd-333f-e063-6294a90a3505 2026-07-08 Warnings Exact identifier application number: M017 Natures Willow Balm MENTHOL WB VENTURES LLC b9f50c43-b0d5-39a8-e053-2995a90a04f1 2026-07-08 Warnings Exact identifier application number: M017 Natures Willow Bug Bite Balm MENTHOL WB Ventures LLC b9fab18f-32c7-d5bd-e053-2995a90a6d0f 2026-07-08 Warnings Exact identifier application number: M017 Salonpas pain relieving hot CAPSAICIN, MENTHOL Hisamitsu Pharmaceutical Co., Inc. d2aa8820-a947-404b-b617-e692fbd16502 2026-07-07 Warnings Exact identifier application number: M017 Quali Yi Tiao Gen Pain Patch CAPSAICIN PATCH Sheng Chang Pharmaceutical Co, Ltd. Zhongli Factory 33154a9b-f6d0-4e95-b4cb-6b938f5dcf4d 2026-07-07 Warnings Exact identifier application number: M017 MUYOHON Numbing Cream NUMBING CREAM Guangzhou Jingliang Cosmetics Co., Ltd. 55caf0a5-f062-a6c3-e063-6294a90ae073 2026-07-04 Warnings Exact identifier application number: M017 Targeted Warming Capsaicin Patch CAPSAICIN Army & Air Force Exchange Service 55b539f8-38c4-594e-e063-6394a90afbaa 2026-07-03 Warnings Exact identifier application number: M017 TopCare Health Pain Relief LIDOCAINE HYDROCHLORIDE Topco Associates LLC 485b0671-da09-19d7-e063-6294a90aca5d 2026-07-03 Warnings Exact identifier application number: M017 Mineral Ice Methol Pain Relief MENTHOL 10.5 % Sunflora Inc 6ddd9e97-f717-4d5a-9658-26449a3cc831 2026-07-02 Warnings Exact identifier application number: M017 Burn Relief LIDOCAINE AmerisourceBergen Drug Corporation 7d898e33-ded7-c9b9-e053-2a91aa0adf7c 2026-07-01 Warnings Exact identifier application number: M017 Desert Harvest Releveum with Lidocaine LIDOCAINE HYDROCHLORIDE Desert Harvest, Inc 9ad514ab-a6bd-4564-8ba3-0149032ebf36 2026-07-01 Warnings Exact identifier application number: M017 CVS No Mess Cortisone HYDROCORTISONE Natural Essentials, Inc. 558c94ec-95f1-eb98-e063-6394a90a1e72 2026-07-01 Warnings Exact identifier application number: M017 MUSCLE EASE MENTHOL CAMPHOR SOMBRA COSMETICS INC. 03fff4bf-04ed-49a6-b40f-4d98c2b42f69 2026-07-01 Warnings Exact identifier application number: M017 OrthoNesic Pain Relieving Gel MENTHOL, CAMPHOR Blaine Labs Inc. 122f60c2-f8df-4625-8bb8-a2244a261b5d 2026-07-01 Warnings Exact identifier application number: M017 Desert Harvest RELEVEUM LIDOCAINE Desert Harvest Inc. 5d9010ec-d482-44ff-ba27-3bfec5a241c6 2026-06-30 Warnings Exact identifier application number: M017 Promescent LIDICAINE Absorption 5b508238-3be7-4b0d-bf35-51de79f58f55 2026-06-30 Warnings Exact identifier application number: M017 Lidovyx LIDOCAINE 4% V2 Pharma LLC 4465eb60-a617-4608-9504-8b3b4c64f49e 2026-06-30 Warnings Exact identifier application number: M017 Dr.Johnes Lidocaine 4% Topical Analgesic Cream LIDOCAINE HCL,MENTHOL Dr.Johnes LLC 6144708d-4b0f-4f0d-88e3-6925ba2d004d 2026-06-29 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 69396-023-01 69396002301 1 TUBE in 1 BOX (69396-023-01) / 28.4 g in 1 TUBE 1 tube 2022-09-14 0000-00-00 No No Current