KENS PAIN AND ARTHRITIS FORMULA
- Product NDC
- 69678-143
- 11-digit product format
- 696780143
- Labeler code
- 69678
- Product ID
- 69678-143_c01c4dab-9263-43d7-88dd-5df72403f96c
- 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
- Substance
- MENTHOL, UNSPECIFIED FORM
- Active strength
- 2.75 g/100mL
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- KENS PAIN AND ARTHRITIS FORMULA
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| MENTHOL, UNSPECIFIED FORM | 2.75 g/100mL |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | L7T10EIP3A |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| 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#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 69678-143 | KENS PAIN AND ARTHRITIS FORMULA (MENTHOL) LIQUID [EEZAWAY RELIEF INC] | 1 | Current NDC, 1 package rows | 20240308_35834473-3ad5-41ec-a110-e742aa7e2ee4.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 69678-143-03 | 69678014303 | 88 mL in 1 BOTTLE (69678-143-03) | 88 ml | 2024-03-05 | No | No | Historical |