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Bengay Ultra Strength Pain Relieving
Bengay Ultra Strength Pain Relieving - 58232-4024-5 - (Camphor (Synthetic), Menthol, and Methyl Salicylate)
Drug Information of Bengay Ultra Strength Pain Relieving
| Product NDC: | 58232-4024 |
| Proprietary Name: | Bengay Ultra Strength Pain Relieving |
| Non Proprietary Name: | Camphor (Synthetic), Menthol, and Methyl Salicylate |
| Active Ingredient(s): | 40; 100; 300 mg/g; mg/g; mg/g & nbsp; Camphor (Synthetic), Menthol, and Methyl Salicylate |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | CREAM |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Bengay Ultra Strength Pain Relieving
| Product NDC: | 58232-4024 |
| 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: | 20120807 |
Package Information of Bengay Ultra Strength Pain Relieving
| Package NDC: | 58232-4024-5 |
| Package Description: | 1 TUBE in 1 CARTON (58232-4024-5) > 76 g in 1 TUBE |
NDC Information of Bengay Ultra Strength Pain Relieving
| NDC Code | 58232-4024-5 |
| Proprietary Name | Bengay Ultra Strength Pain Relieving |
| Package Description | 1 TUBE in 1 CARTON (58232-4024-5) > 76 g in 1 TUBE |
| Product NDC | 58232-4024 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Camphor (Synthetic), Menthol, and Methyl Salicylate |
| Dosage Form Name | CREAM |
| Route Name | TOPICAL |
| Start Marketing Date | 20120807 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Johnson & Johnson Consumer Products Company, Division of Johnson & Johnson Consumer Companies, Inc. |
| Substance Name | CAMPHOR (SYNTHETIC); MENTHOL; METHYL SALICYLATE |
| Strength Number | 40; 100; 300 |
| Strength Unit | mg/g; mg/g; mg/g |
| Pharmaceutical Classes |
