| Product NDC: | 58232-0711 |
| Proprietary Name: | Neosporin Plus Pain Relief Neo To Go First Aid Antiseptic Pain Relieving |
| Non Proprietary Name: | BENZALKONIUM CHLORIDE AND PRAMOXINE HYDROCHLORIDE |
| Active Ingredient(s): | 1.3; 10 mg/mL; mg/mL & nbsp; BENZALKONIUM CHLORIDE AND PRAMOXINE HYDROCHLORIDE |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | SPRAY |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 58232-0711 |
| Labeler Name: | Johnson & Johnson Consumer Products Company, Division of Johnson & Johnson Consumer Companies, Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part347 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20130627 |
| Package NDC: | 58232-0711-1 |
| Package Description: | 1 VIAL in 1 BLISTER PACK (58232-0711-1) > 7.7 mL in 1 VIAL |
| NDC Code | 58232-0711-1 |
| Proprietary Name | Neosporin Plus Pain Relief Neo To Go First Aid Antiseptic Pain Relieving |
| Package Description | 1 VIAL in 1 BLISTER PACK (58232-0711-1) > 7.7 mL in 1 VIAL |
| Product NDC | 58232-0711 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | BENZALKONIUM CHLORIDE AND PRAMOXINE HYDROCHLORIDE |
| Dosage Form Name | SPRAY |
| Route Name | TOPICAL |
| Start Marketing Date | 20130627 |
| 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; PRAMOXINE HYDROCHLORIDE |
| Strength Number | 1.3; 10 |
| Strength Unit | mg/mL; mg/mL |
| Pharmaceutical Classes |