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Superior Analgesic
Superior Analgesic - 58350-000-00 - (Superior Analgesic)
Drug Information of Superior Analgesic
| Product NDC: | 58350-000 |
| Proprietary Name: | Superior Analgesic |
| Non Proprietary Name: | Superior Analgesic |
| Active Ingredient(s): | 3.5 mg/100mL & nbsp; Superior Analgesic |
| Administration Route(s): | TRANSDERMAL |
| Dosage Form(s): | LINIMENT |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Superior Analgesic
| Product NDC: | 58350-000 |
| Labeler Name: | Superior Trading Company |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part346 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20091228 |
Package Information of Superior Analgesic
| Package NDC: | 58350-000-00 |
| Package Description: | 100 mL in 1 BOTTLE (58350-000-00) |
NDC Information of Superior Analgesic
| NDC Code | 58350-000-00 |
| Proprietary Name | Superior Analgesic |
| Package Description | 100 mL in 1 BOTTLE (58350-000-00) |
| Product NDC | 58350-000 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Superior Analgesic |
| Dosage Form Name | LINIMENT |
| Route Name | TRANSDERMAL |
| Start Marketing Date | 20091228 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Superior Trading Company |
| Substance Name | MENTHOL |
| Strength Number | 3.5 |
| Strength Unit | mg/100mL |
| Pharmaceutical Classes |
