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ORAGESIC Oral Pain Reliever
ORAGESIC Oral Pain Reliever - 50930-099-08 - (BENZYL ALCOHOL, MENTHOL)
Drug Information of ORAGESIC Oral Pain Reliever
| Product NDC: | 50930-099 |
| Proprietary Name: | ORAGESIC Oral Pain Reliever |
| Non Proprietary Name: | BENZYL ALCOHOL, MENTHOL |
| Active Ingredient(s): | 10; .4 mg/mL; mg/mL & nbsp; BENZYL ALCOHOL, MENTHOL |
| Administration Route(s): | ORAL |
| Dosage Form(s): | SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of ORAGESIC Oral Pain Reliever
| Product NDC: | 50930-099 |
| Labeler Name: | Parnell Pharmaceuticals Inc |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part356 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20130102 |
Package Information of ORAGESIC Oral Pain Reliever
| Package NDC: | 50930-099-08 |
| Package Description: | 237 mL in 1 BOTTLE (50930-099-08) |
NDC Information of ORAGESIC Oral Pain Reliever
| NDC Code | 50930-099-08 |
| Proprietary Name | ORAGESIC Oral Pain Reliever |
| Package Description | 237 mL in 1 BOTTLE (50930-099-08) |
| Product NDC | 50930-099 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | BENZYL ALCOHOL, MENTHOL |
| Dosage Form Name | SOLUTION |
| Route Name | ORAL |
| Start Marketing Date | 20130102 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Parnell Pharmaceuticals Inc |
| Substance Name | BENZYL ALCOHOL; MENTHOL |
| Strength Number | 10; .4 |
| Strength Unit | mg/mL; mg/mL |
| Pharmaceutical Classes |
