Ultra Strength Pain Relief is a Topical Spray in the Human Otc Drug category. It is labeled and distributed by Product Quest Mfg. The primary component is Camphor (synthetic); Menthol; Methyl Salicylate.
| Product ID | 64048-5114_2c4c25cc-4283-435e-a614-1cad8d1338f6 |
| NDC | 64048-5114 |
| Product Type | Human Otc Drug |
| Proprietary Name | Ultra Strength Pain Relief |
| Generic Name | Camphor 4%, Menthol 10%, Methyl Salicylate 30% |
| Dosage Form | Spray |
| Route of Administration | TOPICAL |
| Marketing Start Date | 2014-02-06 |
| Marketing Category | OTC MONOGRAPH NOT FINAL / OTC MONOGRAPH NOT FINAL |
| Application Number | part348 |
| Labeler Name | Product Quest Mfg |
| Substance Name | CAMPHOR (SYNTHETIC); MENTHOL; METHYL SALICYLATE |
| Active Ingredient Strength | 4 g/100g; g/100g; g/100g |
| NDC Exclude Flag | N |
| Listing Certified Through | 2019-12-31 |
| Marketing Start Date | 2014-02-06 |
| NDC Exclude Flag | N |
| Sample Package? | N |
| Marketing Category | OTC monograph not final |
| Application Number | part348 |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2014-02-06 |
| Inactivation Date | 2020-01-31 |
| Ingredient | Strength |
|---|---|
| CAMPHOR (SYNTHETIC) | 4 g/100g |
| SPL SET ID: | 4a595401-20af-437e-a658-44e9358d9008 |
| Manufacturer | |
| UNII | |
| RxNorm Concept Unique ID - RxCUI | |
| UPC Code |
| NDC | Brand Name | Generic Name |
|---|---|---|
| 41520-317 | Ultra Strength Pain Relief | Camphor 4%, Menthol 10%, Methyl Salicylate 30% |
| 52000-135 | ULTRA STRENGTH PAIN RELIEF | capsaicin |
| 64048-5114 | Ultra Strength Pain Relief | Camphor 4%, Menthol 10%, Methyl Salicylate 30% |
| 71183-135 | ULTRA STRENGTH PAIN RELIEF | capsaicin |
| 72839-147 | Warrior Pain Relieving | Camphor 4%, Menthol 10%, Methyl Salicylate 30% |