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Sunmark Nose
Sunmark Nose - 49348-197-27 - (Phenylephrine hydrochloride)
Drug Information of Sunmark Nose
| Product NDC: | 49348-197 |
| Proprietary Name: | Sunmark Nose |
| Non Proprietary Name: | Phenylephrine hydrochloride |
| Active Ingredient(s): | 1 mL/100mL & nbsp; Phenylephrine hydrochloride |
| Administration Route(s): | NASAL |
| Dosage Form(s): | LIQUID |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Sunmark Nose
| Product NDC: | 49348-197 |
| Labeler Name: | McKesson |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part341 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20030821 |
Package Information of Sunmark Nose
| Package NDC: | 49348-197-27 |
| Package Description: | 1 BOTTLE, DROPPER in 1 CARTON (49348-197-27) > 30 mL in 1 BOTTLE, DROPPER |
NDC Information of Sunmark Nose
| NDC Code | 49348-197-27 |
| Proprietary Name | Sunmark Nose |
| Package Description | 1 BOTTLE, DROPPER in 1 CARTON (49348-197-27) > 30 mL in 1 BOTTLE, DROPPER |
| Product NDC | 49348-197 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Phenylephrine hydrochloride |
| Dosage Form Name | LIQUID |
| Route Name | NASAL |
| Start Marketing Date | 20030821 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | McKesson |
| Substance Name | PHENYLEPHRINE HYDROCHLORIDE |
| Strength Number | 1 |
| Strength Unit | mL/100mL |
| Pharmaceutical Classes |
