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 |