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Sunmark Nasal
Sunmark Nasal - 49348-028-27 - (oxymetazoline hydrochloride)
Drug Information of Sunmark Nasal
| Product NDC: | 49348-028 |
| Proprietary Name: | Sunmark Nasal |
| Non Proprietary Name: | oxymetazoline hydrochloride |
| Active Ingredient(s): | .5 mg/mL & nbsp; oxymetazoline hydrochloride |
| Administration Route(s): | NASAL |
| Dosage Form(s): | SPRAY |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Sunmark Nasal
| Product NDC: | 49348-028 |
| Labeler Name: | McKesson |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part341 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20030627 |
Package Information of Sunmark Nasal
| Package NDC: | 49348-028-27 |
| Package Description: | 1 BOTTLE, SPRAY in 1 CARTON (49348-028-27) > 30 mL in 1 BOTTLE, SPRAY |
NDC Information of Sunmark Nasal
| NDC Code | 49348-028-27 |
| Proprietary Name | Sunmark Nasal |
| Package Description | 1 BOTTLE, SPRAY in 1 CARTON (49348-028-27) > 30 mL in 1 BOTTLE, SPRAY |
| Product NDC | 49348-028 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | oxymetazoline hydrochloride |
| Dosage Form Name | SPRAY |
| Route Name | NASAL |
| Start Marketing Date | 20030627 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | McKesson |
| Substance Name | OXYMETAZOLINE HYDROCHLORIDE |
| Strength Number | .5 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes |
