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Banalg
Banalg - 21695-440-02 - (Methyl Salicylate)
Drug Information of Banalg
| Product NDC: | 21695-440 |
| Proprietary Name: | Banalg |
| Non Proprietary Name: | Methyl Salicylate |
| Active Ingredient(s): | 30; 140 mg/g; mg/g & nbsp; Methyl Salicylate |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | LOTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Banalg
| Product NDC: | 21695-440 |
| Labeler Name: | Rebel Distributors Corp |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part348 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20070101 |
Package Information of Banalg
| Package NDC: | 21695-440-02 |
| Package Description: | 60 g in 1 BOTTLE (21695-440-02) |
NDC Information of Banalg
| NDC Code | 21695-440-02 |
| Proprietary Name | Banalg |
| Package Description | 60 g in 1 BOTTLE (21695-440-02) |
| Product NDC | 21695-440 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Methyl Salicylate |
| Dosage Form Name | LOTION |
| Route Name | TOPICAL |
| Start Marketing Date | 20070101 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Rebel Distributors Corp |
| Substance Name | MENTHOL; METHYL SALICYLATE |
| Strength Number | 30; 140 |
| Strength Unit | mg/g; mg/g |
| Pharmaceutical Classes |
