Product NDC: | 0113-0304 |
Proprietary Name: | Good Sense Nasal |
Non Proprietary Name: | oxymetazoline hydrochloride |
Active Ingredient(s): | .5 mg/mL & nbsp; oxymetazoline hydrochloride |
Administration Route(s): | NASAL |
Dosage Form(s): | LIQUID |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 0113-0304 |
Labeler Name: | L Perrigo Company |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part341 |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 19890915 |
Package NDC: | 0113-0304-10 |
Package Description: | 1 BOTTLE, SPRAY in 1 CARTON (0113-0304-10) > 30 mL in 1 BOTTLE, SPRAY |
NDC Code | 0113-0304-10 |
Proprietary Name | Good Sense Nasal |
Package Description | 1 BOTTLE, SPRAY in 1 CARTON (0113-0304-10) > 30 mL in 1 BOTTLE, SPRAY |
Product NDC | 0113-0304 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | oxymetazoline hydrochloride |
Dosage Form Name | LIQUID |
Route Name | NASAL |
Start Marketing Date | 19890915 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | L Perrigo Company |
Substance Name | OXYMETAZOLINE HYDROCHLORIDE |
Strength Number | .5 |
Strength Unit | mg/mL |
Pharmaceutical Classes |