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Up and up nasal
Up and up nasal - 11673-304-10 - (oxymetazoline hydrochloride)
Drug Information of Up and up nasal
| Product NDC: | 11673-304 |
| Proprietary Name: | Up and up nasal |
| Non Proprietary Name: | oxymetazoline hydrochloride |
| Active Ingredient(s): | .05 g/100mL & nbsp; oxymetazoline hydrochloride |
| Administration Route(s): | NASAL |
| Dosage Form(s): | SPRAY |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Up and up nasal
| Product NDC: | 11673-304 |
| Labeler Name: | Target Corporation |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part341 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20090812 |
Package Information of Up and up nasal
| Package NDC: | 11673-304-10 |
| Package Description: | 1 BOTTLE, SPRAY in 1 CARTON (11673-304-10) > 30 mL in 1 BOTTLE, SPRAY |
NDC Information of Up and up nasal
| NDC Code | 11673-304-10 |
| Proprietary Name | Up and up nasal |
| Package Description | 1 BOTTLE, SPRAY in 1 CARTON (11673-304-10) > 30 mL in 1 BOTTLE, SPRAY |
| Product NDC | 11673-304 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | oxymetazoline hydrochloride |
| Dosage Form Name | SPRAY |
| Route Name | NASAL |
| Start Marketing Date | 20090812 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Target Corporation |
| Substance Name | OXYMETAZOLINE HYDROCHLORIDE |
| Strength Number | .05 |
| Strength Unit | g/100mL |
| Pharmaceutical Classes |
