Home
>
National Drug Code (NDC)
>
Mountain Series Weekender Medical
Mountain Series Weekender Medical - 44224-0118-1 - (BENZALKONIUM CHLORIDE, POVIDONE-IODINE, ACETAMINOPHEN, ASPIRIN, DIPHENHYDRAMINE HYDROCHLORIDE, IBUPROFEN, BACITRACIN ZINC, NEOMYCIN SULFATE, POLYMYXIN B SULFATE)
Drug Information of Mountain Series Weekender Medical
| Product NDC: | 44224-0118 |
| Proprietary Name: | Mountain Series Weekender Medical |
| Non Proprietary Name: | BENZALKONIUM CHLORIDE, POVIDONE-IODINE, ACETAMINOPHEN, ASPIRIN, DIPHENHYDRAMINE HYDROCHLORIDE, IBUPROFEN, BACITRACIN ZINC, NEOMYCIN SULFATE, POLYMYXIN B SULFATE |
| Active Ingredient(s): | & nbsp; BENZALKONIUM CHLORIDE, POVIDONE-IODINE, ACETAMINOPHEN, ASPIRIN, DIPHENHYDRAMINE HYDROCHLORIDE, IBUPROFEN, BACITRACIN ZINC, NEOMYCIN SULFATE, POLYMYXIN B SULFATE |
| Administration Route(s): | |
| Dosage Form(s): | KIT |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Mountain Series Weekender Medical
| Product NDC: | 44224-0118 |
| Labeler Name: | Tender Corporation dba Adventure Medical Kits |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part333A |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20110801 |
Package Information of Mountain Series Weekender Medical
| Package NDC: | 44224-0118-1 |
| Package Description: | 1 KIT in 1 KIT (44224-0118-1) * .8 mL in 1 PACKAGE (52124-0001-1) * .5 g in 1 TUBE (52124-0003-1) * 2 TABLET, FILM COATED in 1 PACKET (47682-116-99) * 1 CAPSULE in 1 PACKET (47682-182-46) * 2 TABLET, FILM COATED in 1 PACKET (47682-808-99) * 2 TABLET, FILM COATED in 1 PACKET (47682-145-99) * 22 g in 1 PACKET (52380-0001-3) |
NDC Information of Mountain Series Weekender Medical
| NDC Code | 44224-0118-1 |
| Proprietary Name | Mountain Series Weekender Medical |
| Package Description | 1 KIT in 1 KIT (44224-0118-1) * .8 mL in 1 PACKAGE (52124-0001-1) * .5 g in 1 TUBE (52124-0003-1) * 2 TABLET, FILM COATED in 1 PACKET (47682-116-99) * 1 CAPSULE in 1 PACKET (47682-182-46) * 2 TABLET, FILM COATED in 1 PACKET (47682-808-99) * 2 TABLET, FILM COATED in 1 PACKET (47682-145-99) * 22 g in 1 PACKET (52380-0001-3) |
| Product NDC | 44224-0118 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | BENZALKONIUM CHLORIDE, POVIDONE-IODINE, ACETAMINOPHEN, ASPIRIN, DIPHENHYDRAMINE HYDROCHLORIDE, IBUPROFEN, BACITRACIN ZINC, NEOMYCIN SULFATE, POLYMYXIN B SULFATE |
| Dosage Form Name | KIT |
| Route Name | |
| Start Marketing Date | 20110801 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Tender Corporation dba Adventure Medical Kits |
| Substance Name | |
| Strength Number | |
| Strength Unit | |
| Pharmaceutical Classes |
