Leader Roll-On Cooling Pain Relief
- Product NDC
- 70000-0617
- 11-digit product format
- 700000617
- Labeler code
- 70000
- Product ID
- 70000-0617_f835accf-f50d-4831-b28f-881db7ed2e01
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- MENTHOL, UNSPECIFIED FORM
- Dosage form
- GEL
- Route
- TOPICAL
- Labeler
- Cardinal Health, 110 dba LEADER
- Application
- M017
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2022-11-03
- Substance
- MENTHOL, UNSPECIFIED FORM
- Active strength
- 40 mg/mL
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Leader Roll-On Cooling Pain Relief
- Brand name suffix
- Topical Analgesic
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| MENTHOL, UNSPECIFIED FORM | 40 mg/mL |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | L7T10EIP3A |
| Rxcui | 415974 |
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 70000-0617-1 | Leader Roll-On Cooling Pain ReliefTopical Analgesic | 74 mL in 1 BOTTLE, WITH APPLICATOR | GEL | 74 | | 3 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 70000-0617 | LEADER ROLL-ON COOLING PAIN RELIEF TOPICAL ANALGESIC (MENTHOL, UNSPECIFIED FORM) GEL [CARDINAL HEALTH, 110 DBA LEADER] | 2 | Current NDC, Legacy NDC, 1 package rows | 20240302_e86cba40-6b10-454d-98b3-6b547456eaad.zip |
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 |
|---|
| 70000-0617-1 | 70000061701 | 74 mL in 1 BOTTLE, WITH APPLICATOR (70000-0617-1) | 74 ml | 2022-11-03 | 0000-00-00 | No | No | Current |