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Bengay Ultra Strength
Bengay Ultra Strength - 58232-6000-5 - (Menthol)
Drug Information of Bengay Ultra Strength
| Product NDC: | 58232-6000 |
| Proprietary Name: | Bengay Ultra Strength |
| Non Proprietary Name: | Menthol |
| Active Ingredient(s): | 50 mg/1 & nbsp; Menthol |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | PATCH |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Bengay Ultra Strength
| Product NDC: | 58232-6000 |
| Labeler Name: | Johnson & Johnson Consumer Products Company, Division of Johnson & Johnson Consumer Companies, Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part348 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20120901 |
Package Information of Bengay Ultra Strength
| Package NDC: | 58232-6000-5 |
| Package Description: | 5 POUCH in 1 CARTON (58232-6000-5) > 1 PATCH in 1 POUCH |
NDC Information of Bengay Ultra Strength
| NDC Code | 58232-6000-5 |
| Proprietary Name | Bengay Ultra Strength |
| Package Description | 5 POUCH in 1 CARTON (58232-6000-5) > 1 PATCH in 1 POUCH |
| Product NDC | 58232-6000 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Menthol |
| Dosage Form Name | PATCH |
| Route Name | TOPICAL |
| Start Marketing Date | 20120901 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Johnson & Johnson Consumer Products Company, Division of Johnson & Johnson Consumer Companies, Inc. |
| Substance Name | MENTHOL |
| Strength Number | 50 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |
