KENS PAIN AND ARTHRITIS FORMULA

Product NDC
69678-143
11-digit product format
696780143
Labeler code
69678
Product ID
69678-143_a5aa2c6d-88b9-49f7-bf78-1c193f3413fc
Type
HUMAN OTC DRUG
Nonproprietary name
MENTHOL
Dosage form
LIQUID
Route
TOPICAL
Labeler
Eezaway Relief Inc
Application
M017
Marketing category
OTC MONOGRAPH DRUG
Marketing start
2024-03-05
Marketing end
2027-01-31
Substance
MENTHOL, UNSPECIFIED FORM
Active strength
2.75 g/100mL
NDC exclude flag
No
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
KENS PAIN AND ARTHRITIS FORMULA

Active Ingredients#

Ingredient, Strength table
IngredientStrength
MENTHOL, UNSPECIFIED FORM2.75 g/100mL

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
L7T10EIP3AInternal UNII lookup

Harmonized SPL set identifiers#

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

Identifier, FDA.report destination table
IdentifierFDA.report destination
35834473-3ad5-41ec-a110-e742aa7e2ee4Available on FDA.report

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
6c13b22c-b3ba-4127-b768-0132dd5ab0d1Product name120230829
5f30b278-5791-4113-8781-878a9221ef8aProduct name220230125
2a70c781-a755-4d76-b20a-a958acfbdcdcProduct name220190619
304592ef-4a8a-4c22-8e8c-af73aa3d60e5Product name120180703
ac0821a1-ce75-4ea7-880a-59eecaecdf22Product name120180703
db5dc4f9-b907-46f6-8fb7-babcf04bbe5cProduct name120180619
4073022c-5d5d-48f5-82ed-091ad146a4b2Product name120171211
41e9d6cf-3ed7-4c44-a57e-0685058d0896Product name120170824
5e652c92-68fd-426b-b0e7-5fc64e0b9f99Product name120170309
9ffbd0ae-0bce-c086-b707-f0da5f8cd7c5Product name120150828
ddc0c11a-bba8-408f-b3c7-c4828b4bcc8cProduct name120150421

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
69678-143-03KENS PAIN AND ARTHRITIS FORMULA88 mL in 1 BOTTLELIQUID882

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
69678-143KENS PAIN AND ARTHRITIS FORMULA (MENTHOL) LIQUID [EEZAWAY RELIEF INC]1Current NDC, 1 package rows20240308_35834473-3ad5-41ec-a110-e742aa7e2ee4.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 50 of 153 · 3,057 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
PAIN RELIEF PATCHESLIDOCAINEAhold U.S.A., Inc,7e7a813e-424d-4a78-9c72-541c3c62606a2025-12-28WarningsExact identifier
application number: M017
Amazon Basics Cold and Hot Medicated PatchMENTHOLAmazon.com Services LLCe3b4db12-c846-b984-e053-2a95a90a8e9a2025-12-28WarningsExact identifier
application number: M017
Amazon Basics Pain Relief Patch with 4% LidocaineLIDOCAINEAmazon.com Services LLCe3b4f9b1-ac6b-cb2a-e053-2a95a90a9e1e2025-12-28WarningsExact identifier
application number: M017
Absorbine Jr Neck and ShoulderABSORBINE JR NECK AND SHOULDERClarion Brands LLC22f2f191-9146-3075-e063-6394a90aef5f2025-12-28WarningsExact identifier
application number: M017
Absorbine Jr. Pain Relieving Knee PatchABSORBINE JR. PAIN RELIEVING KNEE PATCHClarion Brands, LLC22f71254-e521-2d82-e063-6394a90a12d82025-12-28WarningsExact identifier
application number: M017
Absorbine Jr Back PatchABSORBINE JR BACK PATCHClarion Brands LLC.22f5147e-ff2b-4ae8-e063-6394a90a4e542025-12-28WarningsExact identifier
application number: M017
Absorbine Jr. Pro RollonABSORBINE JR. PRO ROLLONClarion Brands, LLC470efcd0-d350-3dc4-e063-6394a90ab8c12025-12-28WarningsExact identifier
application number: M017
Med Rub BalmACHES AND PAIN BALMWellmetech Pharmaceutical Industries SDN BHDa5801566-6bbe-44f6-8761-9c1ce30969002025-12-27WarningsExact identifier
application number: M017
N-Labs ArcticZen Pain Relief KneeCAMPHOR (SYNTHETIC), MENTHOLNutriomo Labs PTE., LTD46e92db7-a48b-2c7a-e063-6394a90a438e2025-12-27WarningsExact identifier
application number: M017
Absorbine Jr. PlusMENTHOLClarion Brands, LLC46f4ad3c-7418-a6bf-e063-6394a90a4eb82025-12-27WarningsExact identifier
application number: M017
Equate Lidocaine Cool and HeatLIDOCAINE 4% PLUS MENTHOL 1%Walmart Stores Incb86769c3-a0b4-c481-e053-2a95a90af38b2025-12-27WarningsExact identifier
application number: M017
Medicated Body Extra Strength PowderMENTHOL 0.80%Walmart Stores Incb0786418-7b28-d316-e053-2995a90a3ab52025-12-27WarningsExact identifier
application number: M017
Maximum Strength Medicated Foot PowderMEDICATED FOOT POWDERWalmart Stores Incb0794d48-eb8b-55c9-e053-2995a90a5b382025-12-27WarningsExact identifier
application number: M017
Walgreens 24-Hour Lidocaine PatchLIDOCAINE 4%Walgreens Companyb8402924-b5fc-0acd-e053-2a95a90a18052025-12-27WarningsExact identifier
application number: M017
Frankincense and Myrrh Foot Pain ReliefMENTHOLWISE CONSUMER PRODUCTS CO.115f1abc-34aa-3c20-e063-6294a90a97642025-12-26WarningsExact identifier
application number: M017
Soothing Nerve ReliefMENTHOLWise Consumer Products46e23c95-1a36-214e-e063-6394a90a98a82025-12-26WarningsExact identifier
application number: M017
Frankincense and Myrrh Foot Pain Relief Combo PackMENTHOLWISE CONSUMER PRODUCTS CO.46e2c8b6-bd94-7100-e063-6294a90ac9982025-12-26WarningsExact identifier
application number: M017
Pain Patch Perfecto 24 Hours Lidocaine 4 % PatchLIDOCAINEPainpatchperfecto LLCa281c3e9-1c48-4905-98cc-3cedf6042adc2025-12-25WarningsExact identifier
application number: M017
Aloe UP SPF 33 MineralZINC OXIDEAloe Care International, LLC35aa6196-682d-8f32-e063-6394a90aad992025-12-24WarningsExact identifier
application number: M017
ETADERM Numbing CreamLIDOCAINENUEPHASE LLC5292c6ff-b878-4e71-878b-4bf08207612e2025-12-24WarningsExact identifier
application number: M017

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
69678-143-036967801430388 mL in 1 BOTTLE (69678-143-03) 88 ml2024-03-052027-01-31NoNoHistorical