Product NDC: | 62750-005 |
Proprietary Name: | Zicam |
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) |
Product NDC: | 62750-005 |
Labeler Name: | Matrixx Initiatives, Inc. |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part341 |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 20100701 |
Package NDC: | 62750-005-11 |
Package Description: | 1 BOTTLE, PLASTIC in 1 CARTON (62750-005-11) > 22.5 mL in 1 BOTTLE, PLASTIC |
NDC Code | 62750-005-11 |
Proprietary Name | Zicam |
Package Description | 1 BOTTLE, PLASTIC in 1 CARTON (62750-005-11) > 22.5 mL in 1 BOTTLE, PLASTIC |
Product NDC | 62750-005 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | oxymetazoline Hydrochloride |
Dosage Form Name | SPRAY |
Route Name | NASAL |
Start Marketing Date | 20100701 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | Matrixx Initiatives, Inc. |
Substance Name | OXYMETAZOLINE HYDROCHLORIDE |
Strength Number | .5 |
Strength Unit | mg/mL |
Pharmaceutical Classes |