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 |
|---|---|
| MENTHOL, UNSPECIFIED FORM | 2.75 g/100mL |
Harmonized UNII identifiers#
| Identifier | FDA.report destination |
|---|---|
| L7T10EIP3A | Internal UNII lookup |
Harmonized SPL set identifiers#
| Identifier | FDA.report destination |
|---|---|
| 35834473-3ad5-41ec-a110-e742aa7e2ee4 | Available on FDA.report |
DailyMed Product Concepts#
| Product concept | Relation | Version | Effective |
|---|---|---|---|
| 6c13b22c-b3ba-4127-b768-0132dd5ab0d1 | Product name | 1 | 20230829 |
| 5f30b278-5791-4113-8781-878a9221ef8a | Product name | 2 | 20230125 |
| 2a70c781-a755-4d76-b20a-a958acfbdcdc | Product name | 2 | 20190619 |
| 304592ef-4a8a-4c22-8e8c-af73aa3d60e5 | Product name | 1 | 20180703 |
| ac0821a1-ce75-4ea7-880a-59eecaecdf22 | Product name | 1 | 20180703 |
| db5dc4f9-b907-46f6-8fb7-babcf04bbe5c | Product name | 1 | 20180619 |
| 4073022c-5d5d-48f5-82ed-091ad146a4b2 | Product name | 1 | 20171211 |
| 41e9d6cf-3ed7-4c44-a57e-0685058d0896 | Product name | 1 | 20170824 |
| 5e652c92-68fd-426b-b0e7-5fc64e0b9f99 | Product name | 1 | 20170309 |
| 9ffbd0ae-0bce-c086-b707-f0da5f8cd7c5 | Product name | 1 | 20150828 |
| ddc0c11a-bba8-408f-b3c7-c4828b4bcc8c | Product name | 1 | 20150421 |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 69678-143-03 | KENS PAIN AND ARTHRITIS FORMULA | 88 mL in 1 BOTTLE | LIQUID | 88 | 2 |
DailyMed Dashboard NDC Coverage#
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.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| Good Neighbor Pharmacy Hydrocortisone with Aloe | HYDROCORTISONE | AmerisourceBergen | 0c544792-63d9-400c-9888-207c44fdc75e | 2025-07-08 | Warnings | M017 |
| Good Neighbor Pharmacy Hydrocortisone | HYDROCORTISONE | AmerisourceBergen | 58b0b7ba-e547-4e0f-b04d-8e1e6a5d4fcf | 2025-07-08 | Warnings | M017 |
| Publix Hydro | HYDROCORTISONE | Publix Super Markets Inc | 29296b0f-0eed-4bb9-8727-c25c2bcf9fd6 | 2025-07-08 | Warnings | M017 |
| Publix hydro plus | HYDROCORTISONE | Publix Super Markets Inc | a00d82c1-6b09-424a-be78-2603eee3fb9d | 2025-07-08 | Warnings | M017 |
| Tattoo | TATTOO CREAM | Perfso (HK) Co., Limited | 39773cab-12df-4520-e063-6294a90abc5b | 2025-07-08 | Warnings | M017 |
| Neutrogena Sun Rescue After Sun Medicated Relief | CAMPHOR (SYNTHETIC) | Kenvue Brands LLC | c95c5b64-b90f-1143-e053-2a95a90aa03c | 2025-07-07 | Warnings | M017 |
| sunmark Hydrocortisone | HYDROCORTISONE | Strategic Sourcing Services LLC | 210079e9-3d2f-4489-b468-b96b145034ed | 2025-07-07 | Warnings | M017 |
| Relief Gel | LIDOCAINE HCL | Good Clean Love, Inc. | e5fa2265-ccb7-750c-e053-2995a90aa51e | 2025-07-07 | Warnings | M017 |
| Hydrocortisone Plus 12 Moisturizers | HYDROCORTISONE | Sun Pharmaceutical Industries, Inc. | 09ac2749-a60f-4039-8c80-a0d2eaf50c34 | 2025-07-07 | Warnings | M017 |
| Hydrocortisone | HYDROCORTISONE | Sun Pharmaceutical Industries, Inc. | 2ada9ec2-1c28-4da2-8639-07b3193ffb32 | 2025-07-03 | Warnings | M017 |
| Hydrocortisone with Aloe | HYDROCORTISONE | Sun Pharmaceutical Industries, Inc. | caa2fd64-e262-4d7c-ad8a-69f506feba8c | 2025-07-03 | Warnings | M017 |
| Stopain Extra Strength | MENTHOL | Troy Manufacturing, Inc. | 07e9a235-6d10-4407-8729-beaf936e97ad | 2025-07-03 | Warnings | M017 |
| Blue Ice Topical Analgesic Gel | ICE GEL | International Wholesale | 397cd306-078d-5b7d-e063-6294a90a8bbc | 2025-07-03 | Warnings | M017 |
| LIDOCAINE | LIDOCAINE, MENTHOL | Vive Health LLC | 236ccc6d-21b7-6153-e063-6394a90a4634 | 2025-07-02 | Warnings | M017 |
| AsperFlex MAX | LIDOCAINE 4% WITH MENTHOL 1% | Akron Pharma Inc. | ccf6172b-350a-4b78-b844-f84bf17c491f | 2025-07-02 | Warnings | M017 |
| METHYL SALICYLATE 25% | METHYL SALICYLATE | Oncora Pharma, LLC | 3766e3a9-94a8-4c3e-e063-6394a90aa24a | 2025-07-01 | Warnings | M017 |
| Diphenhydramine Hydrochloride and Zinc Acetate | DIPHENHYDRAMINE HYDROCHLORIDE AND ZINC ACETATE | Sun Pharmaceutical Industries, Inc. | c89e3de8-7d71-485c-8fc5-2832d6024f16 | 2025-07-01 | Warnings | M017 |
| Westlake Outdoor Pain and Itch Relieving | LIDOCAINE 4% PAIN AND ITCH RELIEVING | WESTLAKE HB PHARMA | 3c563b28-4f4f-9d0c-e063-6294a90adf73 | 2025-07-01 | Warnings | M017 |
| Cortizone 10 Water Resistant | HYDROCORTISONE | Chattem, Inc. | 118e55e7-241f-44c4-959e-09bf6221bd77 | 2025-07-01 | Warnings | M017 |
| Quit Smoking Nicotine Patches | NICOTINE TRANSDERMAL PATCHES | Shenzhen Paxi Trading Co., Ltd. | 38c1616e-3b09-0669-e063-6294a90a2c86 | 2025-06-29 | Warnings | M017 |
Packages#
| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|---|---|---|---|---|---|---|---|
| 69678-143-03 | 69678014303 | 88 mL in 1 BOTTLE (69678-143-03) | 88 ml | 2024-03-05 | 2027-01-31 | No | No | Historical |