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BAROX
BAROX - 52227-100-01 - (MENTHOL)
Drug Information of BAROX
| Product NDC: | 52227-100 |
| Proprietary Name: | BAROX |
| Non Proprietary Name: | MENTHOL |
| Active Ingredient(s): | 3 g/120mL & nbsp; MENTHOL |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | GEL |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of BAROX
| Product NDC: | 52227-100 |
| Labeler Name: | KTAIGA CO., LTD. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part348 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20120301 |
Package Information of BAROX
| Package NDC: | 52227-100-01 |
| Package Description: | 120 mL in 1 CARTON (52227-100-01) |
NDC Information of BAROX
| NDC Code | 52227-100-01 |
| Proprietary Name | BAROX |
| Package Description | 120 mL in 1 CARTON (52227-100-01) |
| Product NDC | 52227-100 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | MENTHOL |
| Dosage Form Name | GEL |
| Route Name | TOPICAL |
| Start Marketing Date | 20120301 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | KTAIGA CO., LTD. |
| Substance Name | MENTHOL |
| Strength Number | 3 |
| Strength Unit | g/120mL |
| Pharmaceutical Classes |
