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Neosporin
Neosporin - 58232-4018-1 - (Benzalkonium Chloride)
Drug Information of Neosporin
| Product NDC: | 58232-4018 |
| Proprietary Name: | Neosporin |
| Non Proprietary Name: | Benzalkonium Chloride |
| Active Ingredient(s): | 1.3 mg/mL & nbsp; Benzalkonium Chloride |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | LIQUID |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Neosporin
| Product NDC: | 58232-4018 |
| Labeler Name: | Johnson & Johnson Consumer Products Company, Division of Johnson & Johnson Consumer Companies, Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part333A |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20110622 |
Package Information of Neosporin
| Package NDC: | 58232-4018-1 |
| Package Description: | 68 mL in 1 BOTTLE, PUMP (58232-4018-1) |
NDC Information of Neosporin
| NDC Code | 58232-4018-1 |
| Proprietary Name | Neosporin |
| Package Description | 68 mL in 1 BOTTLE, PUMP (58232-4018-1) |
| Product NDC | 58232-4018 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Benzalkonium Chloride |
| Dosage Form Name | LIQUID |
| Route Name | TOPICAL |
| Start Marketing Date | 20110622 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Johnson & Johnson Consumer Products Company, Division of Johnson & Johnson Consumer Companies, Inc. |
| Substance Name | BENZALKONIUM CHLORIDE |
| Strength Number | 1.3 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes |
