Pain Relieving Roll-On
- Product NDC
- 61010-1550
- 11-digit product format
- 610101550
- Labeler code
- 61010
- Product ID
- 61010-1550_10a91ff8-4d59-15dd-e063-6394a90a3aad
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- menthol, unspecified form
- Dosage form
- GEL
- Route
- TOPICAL
- Labeler
- Safetec of America, Inc.
- Application
- M017
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2019-10-07
- Substance
- MENTHOL, UNSPECIFIED FORM
- Active strength
- 7 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
- Pain Relieving Roll-On
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| MENTHOL, UNSPECIFIED FORM | 7 g/100mL |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | L7T10EIP3A |
| Rxcui | 311509 |
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 61010-1550-1 | Pain Relieving Roll-On | 88 mL in 1 BOTTLE | GEL | 88 | | 2 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 61010-1550 | PAIN RELIEVING ROLL-ON (MENTHOL, UNSPECIFIED FORM) GEL [SAFETEC OF AMERICA, INC.] | 2 | Current NDC, Legacy NDC, 1 package rows | 20240214_80118260-9c88-402d-9a90-ecfe62b4b54f.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 |
|---|
| 61010-1550-1 | 61010155001 | 88 mL in 1 BOTTLE (61010-1550-1) | 88 ml | 2019-10-07 | 0000-00-00 | No | No | Current |