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
IngredientStrength
LIDOCAINE40 mg/g

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
98PI200987Internal UNII lookup

Harmonized RxCUI identifiers#

RxCUI identifiers page 1 of 1 · 2 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
1421893Internal RxNorm lookup
1422103Internal RxNorm lookup

Harmonized SPL set identifiers#

SPL set identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
f0e7c92f-8b0b-4045-b659-af9f6e81260fAvailable on FDA.report

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
0496-0882-05LMX45 g in 1 TUBECREAM56
0496-0882-06LMX45 in 1 CARTONCREAM56
0496-0882-07LMX45 in 1 BOXCREAM56
0496-0882-15LMX415 g in 1 TUBECREAM156
0496-0882-30LMX430 g in 1 TUBECREAM306
0496-0882-71LMX41 in 1 BOXCREAM16

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
0496-0882-05GM - Gram0496-0882c8cc6767-ae03-48b9-a6e5-dbbbcb67f3ce12021-07-15
0496-0882-06GM - Gram0496-088222ebe846-b69c-48b8-b5ce-be3599d1376b12012-07-24
0496-0882-07EA - Each0496-08829a795358-5f11-441b-b27d-ef3adcb2e57412012-07-24
0496-0882-15GM - Gram0496-08827da3a277-b0cc-4ca0-b933-24f121dd0d0812012-07-24
0496-0882-30GM - Gram0496-088206d35deb-53ef-4057-83b7-5ece6b46a5fe12012-07-24
0496-0882-71EA - Each0496-088254d93ce4-7bf8-4116-be6f-74ac7102655b12012-07-24

DailyMed Socrata Ingredients#

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
0496-0882LMX4 (LIDOCAINE) CREAM [FERNDALE LABORATORIES, INC.]5Current NDC, Legacy NDC, 6 package rows20241220_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 135 of 152 · 3,029 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Ralli Rapid Pain Relief Roll onMENTHOLTroy Manufacturing, Inc.978d5c2c-fdc4-4d25-83ec-0b9404ec80182024-02-19WarningsExact identifier
application number: M017
11681168 BURN SPRAYDynarex Corporation1183a4f5-f875-dfb0-e063-6394a90af35f2024-02-16WarningsExact identifier
application number: M017
Pain ReliefBENZOCAINESafetec of America, Inc.de84e598-d047-4fae-b2ed-155a3788bc6f2024-02-16WarningsExact identifier
application number: M017
No Mess Hydrocortisone ApplicatorHYDROCORTISONEWalgreen Co.cfefb517-9099-41c4-8a95-74414ca4032c2024-02-16WarningsExact identifier
application number: M017
Analgesic BalmMENTHOL 10%, METHYL SALICYLATE 15%Geri-Care Pharmaceuticals, Corpab9bf09d-bc8c-6d17-e053-2995a90a6c362024-02-14WarningsExact identifier
application number: M017
Natures Oil 16% MentholMENTHOL, UNSPECIFIED FORMNATURAL ESSENTIALS, INC.2fbe23b7-23a3-4f0b-bc08-0205256f5d682024-02-14WarningsExact identifier
application number: M017
Rugby Pain Relieving AnalgesicMENTHOL, UNSPECIFIED FORM AND METHYL SALICYLATERugby Laboratories4c11876c-57ec-4429-a8c4-fb95baa4074a2024-02-13WarningsExact identifier
application number: M017
Itch stopping CreamDIPHENHYDRAMINE HYDROCHLORIDE 2%, ZINC ACETATE 0.1%Trifecta Pharmaceuticals USA, LLC.11368823-d4af-a536-e063-6294a90a7a2e2024-02-12WarningsExact identifier
application number: M017
Walgreens Boil Pain ReliefBOIL PAIN RELIEFWalgreens Companyd11bd769-68d0-4057-bc2a-72719f16011e2024-02-12WarningsExact identifier
application number: M017
CapsaicinCAPSAICINRugby Laboratoriesc5915c84-84a2-46f6-9f97-0d9873e9944a2024-02-12WarningsExact identifier
application number: M017
Leader Ice Blue AnalgesicMENTHOL, UNSPECIFIED FORMCardinal Health, 110 dba LEADER952e56ea-5cbc-4078-bd01-5d3b6864a5ce2024-02-09WarningsExact identifier
application number: M017
Leader Ultra Strength Muscle Rub Topical AnalgesicCAMPHOR (SYNTHETIC), MENTHOL, UNSPECIFIED FORM, AND METHYL SALICYLATECardinal Health, 110 dba LEADER9d99a900-60e0-454c-98e0-2c63eb910cf12024-02-09WarningsExact identifier
application number: M017
Pain RelievingCAMPHOR (NATURAL)J.R. Watkins, LLC.28821ffa-a138-47b5-8857-beadf7a20d432024-02-08WarningsExact identifier
application number: M017
Menthol Camphor Cough Suppressant Topical Analgesic RubCAMPHOR (NATURAL) AND MENTHOL, UNSPECIFIED FORMJ.R. Watkins, LLC.fd0ea70a-ef12-48b1-8d9d-cc5f6417f8542024-02-08WarningsExact identifier
application number: M017
Pain Relieving CoolingMENTHOL, UNSPECIFIED FORMJ.R. Watkins, LLC.3574d48a-b546-4ea7-b470-071bb328de642024-02-08WarningsExact identifier
application number: M017
Advil Targeted ReliefCAMPHOR, CAPSAICIN, MENTHOL, METHYL SALICYLATEHaleon US Holdings LLC16e6be21-7b43-443a-89ec-3bdf0ec0dfc12024-02-08WarningsExact identifier
application number: M017
POINT RELIEF COLD SPOT Pain RelievingMENTHOLFABRICATION ENTERPRISES96f1d592-6cec-412e-a5fd-cf3c4f68644f2024-02-07WarningsExact identifier
application number: M017
Lidocaine HydrochlorideLIDOCAINE HYDROCHLORIDESafetec of America, Inc.1c5eb3b3-79b3-472a-ae36-ec6a7dc729252024-02-07WarningsExact identifier
application number: M017
Lidocaine HydrochlorideLIDOCAINE HYDROCHLORIDESafetec of America, Inc.8eb3e7e2-26e5-430e-89aa-40a0367c637e2024-02-07WarningsExact identifier
application number: M017
Nova Natura Topical AnalgesicCAMPHOR, CAPSICUM OLEORESIN, METHYL SALICYLATESEYITLER KIMYA SANAYI ANONIM SIRKETIabf00f73-f0b1-439e-85aa-bbce8a1ec9202024-02-06WarningsExact identifier
application number: M017

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
1422103L-M-X-4 4 % Topical CreamPSNf0e7c92f-8b0b-4045-b659-af9f6e81260f6
1421893lidocaine 4 % Topical CreamPSNf0e7c92f-8b0b-4045-b659-af9f6e81260f6
1422103lidocaine 40 MG/ML Topical Cream [LMX]SBDf0e7c92f-8b0b-4045-b659-af9f6e81260f6
1421893lidocaine 40 MG/ML Topical CreamSCDf0e7c92f-8b0b-4045-b659-af9f6e81260f6
1422103L-M-X-4 4 % Topical CreamSYf0e7c92f-8b0b-4045-b659-af9f6e81260f6
1422103L-M-X-4 40 MG/ML Topical CreamSYf0e7c92f-8b0b-4045-b659-af9f6e81260f6
1421893lidocaine 4 % Topical CreamSYf0e7c92f-8b0b-4045-b659-af9f6e81260f6
1422103LMX 40 MG/ML Topical CreamSYf0e7c92f-8b0b-4045-b659-af9f6e81260f6

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
0496-0882-05004960882055 g in 1 TUBE (0496-0882-05) 5 g2011-01-030000-00-00NoNoCurrent
0496-0882-06004960882065 TUBE in 1 CARTON (0496-0882-06) / 5 g in 1 TUBE (0496-0882-05) 5 tube2011-01-030000-00-00NoNoCurrent
0496-0882-07004960882075 TUBE in 1 BOX (0496-0882-07) / 5 g in 1 TUBE (0496-0882-05) 5 tube2011-01-030000-00-00NoNoCurrent
0496-0882-150049608821515 g in 1 TUBE (0496-0882-15) 15 g2011-01-030000-00-00NoNoCurrent
0496-0882-300049608823030 g in 1 TUBE (0496-0882-30) 30 g2011-01-030000-00-00NoNoCurrent
0496-0882-71004960882711 TUBE in 1 BOX (0496-0882-71) / 30 g in 1 TUBE (0496-0882-30) 1 tube2011-01-030000-00-00NoNoCurrent