Home NDC 0496-0882 LMX4
Product NDC 0496-0882
11-digit product format 004960882
Labeler code 0496
Product ID 0496-0882_459c9507-ea18-81b1-e063-6394a90a3db4
Type HUMAN OTC DRUG
Nonproprietary name lidocaine
Dosage form CREAM
Route TOPICAL
Labeler Ferndale Laboratories, Inc.
Application M017
Marketing category OTC MONOGRAPH DRUG
Marketing start 2011-01-03
Substance LIDOCAINE
Active strength 40 mg/g
Pharmacologic classes Amide Local Anesthetic [EPC], Amides [CS], Antiarrhythmic [EPC], Local Anesthesia [PE]
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 LMX4
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength LIDOCAINE 40 mg/g
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 98PI200987 Internal UNII lookup
Harmonized RxCUI identifiers# RxCUI identifiers page 1 of 1 · 2 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 1421893 Internal RxNorm lookup 1422103 Internal RxNorm lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Package Descriptions# DailyMed Socrata Ingredients# Ingredient, Type, UNII table Ingredient Type UNII DailyMed label SPL version Uploaded LIDOCAINE ACTIVE INGREDIENT 98PI200987 LMX4 (LIDOCAINE) CREAM [FERNDALE LABORATORIES, INC.] 2 LIDOCAINE ACTIVE MOIETY 98PI200987 LMX4 (LIDOCAINE) CREAM [FERNDALE LABORATORIES, INC.] 2 ALPHA-TOCOPHEROL ACETATE INACTIVE INGREDIENT 9E8X80D2L0 LMX4 (LIDOCAINE) CREAM [FERNDALE LABORATORIES, INC.] 2 BENZYL ALCOHOL INACTIVE INGREDIENT LKG8494WBH LMX4 (LIDOCAINE) CREAM [FERNDALE LABORATORIES, INC.] 2 CARBOMER HOMOPOLYMER TYPE C INACTIVE INGREDIENT 4Q93RCW27E LMX4 (LIDOCAINE) CREAM [FERNDALE LABORATORIES, INC.] 2 CHOLESTEROL INACTIVE INGREDIENT 97C5T2UQ7J LMX4 (LIDOCAINE) CREAM [FERNDALE LABORATORIES, INC.] 2 POLYSORBATE 80 INACTIVE INGREDIENT 6OZP39ZG8H LMX4 (LIDOCAINE) CREAM [FERNDALE LABORATORIES, INC.] 2 PROPYLENE GLYCOL INACTIVE INGREDIENT 6DC9Q167V3 LMX4 (LIDOCAINE) CREAM [FERNDALE LABORATORIES, INC.] 2 TROLAMINE INACTIVE INGREDIENT 9O3K93S3TK LMX4 (LIDOCAINE) CREAM [FERNDALE LABORATORIES, INC.] 2 WATER INACTIVE INGREDIENT 059QF0KO0R LMX4 (LIDOCAINE) CREAM [FERNDALE LABORATORIES, INC.] 2
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 0496-0882 LMX4 (LIDOCAINE) CREAM [FERNDALE LABORATORIES, INC.] 5 Current NDC, Legacy NDC, 6 package rows 20241220_f0e7c92f-8b0b-4045-b659-af9f6e81260f.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 113 of 153 · 3,057 matching rows.
Brand, Generic, Manufacturer table Brand Generic Manufacturer SPL set ID Effective date Available safety fields Join Rite Aid Cala Itch Relief PRAMOXINE HCL 1%, ZINC ACETATE 0.1% Rite Aid e29a9d59-4c7c-81aa-e053-2995a90a7056 2024-12-15 Warnings Exact identifier application number: M017 CVS Roll-On CAPSAISIN 0.1% CVS e8812c49-335e-61ea-e053-2995a90a17aa 2024-12-15 Warnings Exact identifier application number: M017 Good Sense Burn Relief Aloe LIDOCAINE HCL Geiss, Destin & Dunn, Inc b5a7f629-a88d-b49d-e053-2995a90a49fa 2024-12-15 Warnings Exact identifier application number: M017 QC Burn Relief Aloe LIDOCAINE HCL Chain Drug Marketing Association Inc b5e76f0c-0bfe-b13e-e053-2995a90a0861 2024-12-15 Warnings Exact identifier application number: M017 Meijer Burn Relief LIDOCAINE 0.5% Meijer bec60c93-5abd-ee04-e053-2a95a90acb61 2024-12-15 Warnings Exact identifier application number: M017 QC Cool and Heat Roll-On MENTHOL 16% Chain Drug Marketing Association Inc d35e9dfa-8a28-fdb3-e053-2995a90abc52 2024-12-15 Warnings Exact identifier application number: M017 Meijer Cold and Hot Pain Relieving MENTHOL 16% Meijer bec62df3-06c9-a115-e053-2995a90a4267 2024-12-15 Warnings Exact identifier application number: M017 Tommie Copper Pain Relief MENTHOL 16% Tommie Copper, Inc. b4dfa5fa-2d61-db1e-e053-2a95a90a7ac8 2024-12-15 Warnings Exact identifier application number: M017 Pain Relief Liquid Roller CAMPHOR 3.5%, MENTHOL 3.5% Tommie Copper, Inc. c9f0447e-de43-16a5-e053-2995a90a05c1 2024-12-15 Warnings Exact identifier application number: M017 Tommie Copper Pain Relief Maximum Strength TROLAMINE SALICYLATE 10% Tommie Copper, Inc. b622c14f-9bf3-0bbd-e053-2a95a90a2adc 2024-12-15 Warnings Exact identifier application number: M017 Copperlife Pain Relief TROLAMINE SALICYLATE 10% Tommie Copper, Inc. c94d00f9-42ce-1d43-e053-2a95a90a058d 2024-12-15 Warnings Exact identifier application number: M017 Tommie Copper Pain Relief Roller CAMPHOR 3.5%, MENTHOL 3.5% Tommie Copper, Inc. b6c3d6eb-b485-33b8-e053-2a95a90a41e1 2024-12-15 Warnings Exact identifier application number: M017 Tommie Copper Pain Relief Roller CAMPHOR 3.5%, MENTHOL 3.5% Tommie Copper, Inc. b4cd4fed-e8c8-db85-e053-2995a90a708b 2024-12-15 Warnings Exact identifier application number: M017 Copperlife Pain Relief Liquid MENTHOL 16% Tommie Copper, Inc. c93a0139-953b-5523-e053-2a95a90a0b2d 2024-12-15 Warnings Exact identifier application number: M017 Tommie Copper Pain Relief TROLAMINE SALICYLATE 10% Tommie Copper, Inc. ca011b03-a263-1908-e053-2995a90ad970 2024-12-15 Warnings Exact identifier application number: M017 Warrior Chiggerex Relief BENZOCAINE 10% Derma Care Research Labs, LLC dcf2f52b-2295-58e5-e053-2995a90a7fd8 2024-12-15 Warnings Exact identifier application number: M017 Capsaicin Cream CAPSAICIN Trifecta Pharmaceuticals USA LLC def8d341-06a7-0e9b-e053-2995a90a0ad6 2024-12-13 Warnings Exact identifier application number: M017 Mentholatum Original CAMPHOR, MENTHOL The Mentholatum Company 19e4b812-67c6-49fd-833a-b432100363f5 2024-12-13 Warnings Exact identifier application number: M017 Cold and Hot Medicated MENTHOL The Mentholatum Company 85bf425d-59d7-4462-ba46-292145460099 2024-12-13 Warnings Exact identifier application number: M017 Mentholatum Lidocaine Ice LIDOCAINE HCL, MENTHOL The Mentholatum Company 4d74cbab-31cd-4579-9360-6852ee215b5e 2024-12-13 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 0496-0882-05 00496088205 5 g in 1 TUBE (0496-0882-05) 5 g 2011-01-03 0000-00-00 No No Current 0496-0882-06 00496088206 5 TUBE in 1 CARTON (0496-0882-06) / 5 g in 1 TUBE (0496-0882-05) 5 tube 2011-01-03 0000-00-00 No No Current 0496-0882-07 00496088207 5 TUBE in 1 BOX (0496-0882-07) / 5 g in 1 TUBE (0496-0882-05) 5 tube 2011-01-03 0000-00-00 No No Current 0496-0882-15 00496088215 15 g in 1 TUBE (0496-0882-15) 15 g 2011-01-03 0000-00-00 No No Current 0496-0882-30 00496088230 30 g in 1 TUBE (0496-0882-30) 30 g 2011-01-03 0000-00-00 No No Current 0496-0882-71 00496088271 1 TUBE in 1 BOX (0496-0882-71) / 30 g in 1 TUBE (0496-0882-30) 1 tube 2011-01-03 0000-00-00 No No Current