Flexall Pain Relieving is a Topical Gel in the Human Otc Drug category. It is labeled and distributed by Ari-med Pharmaceuticals. The primary component is Menthol.
| Product ID | 63400-1601_9d3bcb94-c8db-b8fe-e053-2995a90a87a5 |
| NDC | 63400-1601 |
| Product Type | Human Otc Drug |
| Proprietary Name | Flexall Pain Relieving |
| Generic Name | Menthol Analgesic |
| Dosage Form | Gel |
| Route of Administration | TOPICAL |
| Marketing Start Date | 1997-01-01 |
| Marketing Category | OTC MONOGRAPH NOT FINAL / OTC MONOGRAPH NOT FINAL |
| Application Number | part348 |
| Labeler Name | Ari-Med Pharmaceuticals |
| Substance Name | MENTHOL |
| Active Ingredient Strength | 0 g/g |
| NDC Exclude Flag | N |
| Listing Certified Through | 2021-12-31 |
| Marketing Start Date | 1997-01-01 |
| NDC Exclude Flag | N |
| Sample Package? | N |
| Marketing Category | OTC monograph not final |
| Application Number | part348 |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 1997-01-01 |
| Marketing Category | OTC monograph not final |
| Application Number | part348 |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 1997-01-01 |
| Ingredient | Strength |
|---|---|
| MENTHOL | .07 g/g |
| SPL SET ID: | e3b9c361-78fc-4c16-acfa-ff30e423215c |
| Manufacturer | |
| UNII | |
| RxNorm Concept Unique ID - RxCUI |
| NDC | Brand Name | Generic Name |
|---|---|---|
| 21695-642 | Flexall Pain Relieving | Menthol |
| 41167-1601 | Flexall Pain Relieving | Menthol |
| 41167-1602 | Flexall Pain Relieving | Menthol |
| 63187-107 | Flexall Pain Relieving | Menthol |
| 63400-1601 | Flexall Pain Relieving | Menthol Analgesic |
| 63400-1602 | Flexall Pain Relieving | Menthol Analgesic |