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nasal - 41268-065-10 - (Oxymetazoline HCl)
Drug Information of nasal
| Product NDC: | 41268-065 |
| Proprietary Name: | nasal |
| Non Proprietary Name: | Oxymetazoline HCl |
| Active Ingredient(s): | .05 g/100mL & nbsp; Oxymetazoline HCl |
| Administration Route(s): | NASAL |
| Dosage Form(s): | SPRAY |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of nasal
| Product NDC: | 41268-065 |
| Labeler Name: | Hannaford Brothers Company |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part341 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20060421 |
Package Information of nasal
| Package NDC: | 41268-065-10 |
| Package Description: | 1 BOTTLE, SPRAY in 1 CARTON (41268-065-10) > 30 mL in 1 BOTTLE, SPRAY |
NDC Information of nasal
| NDC Code | 41268-065-10 |
| Proprietary Name | nasal |
| Package Description | 1 BOTTLE, SPRAY in 1 CARTON (41268-065-10) > 30 mL in 1 BOTTLE, SPRAY |
| Product NDC | 41268-065 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Oxymetazoline HCl |
| Dosage Form Name | SPRAY |
| Route Name | NASAL |
| Start Marketing Date | 20060421 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Hannaford Brothers Company |
| Substance Name | OXYMETAZOLINE HYDROCHLORIDE |
| Strength Number | .05 |
| Strength Unit | g/100mL |
| Pharmaceutical Classes |
