Product NDC: | 49738-430 |
Proprietary Name: | Eye Allergy Relief |
Non Proprietary Name: | Pheniramine Maleate and Naphazoline Hydrochloride |
Active Ingredient(s): | .2675; 3.15 mg/mL; mg/mL & nbsp; Pheniramine Maleate and Naphazoline Hydrochloride |
Administration Route(s): | OPHTHALMIC |
Dosage Form(s): | SOLUTION/ DROPS |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 49738-430 |
Labeler Name: | Kmart Corporation |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | NDA020065 |
Marketing Category: | NDA |
Start Marketing Date: | 20100831 |
Package NDC: | 49738-430-15 |
Package Description: | 1 BOTTLE, DROPPER in 1 CARTON (49738-430-15) > 15 mL in 1 BOTTLE, DROPPER |
NDC Code | 49738-430-15 |
Proprietary Name | Eye Allergy Relief |
Package Description | 1 BOTTLE, DROPPER in 1 CARTON (49738-430-15) > 15 mL in 1 BOTTLE, DROPPER |
Product NDC | 49738-430 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Pheniramine Maleate and Naphazoline Hydrochloride |
Dosage Form Name | SOLUTION/ DROPS |
Route Name | OPHTHALMIC |
Start Marketing Date | 20100831 |
Marketing Category Name | NDA |
Labeler Name | Kmart Corporation |
Substance Name | NAPHAZOLINE HYDROCHLORIDE; PHENIRAMINE MALEATE |
Strength Number | .2675; 3.15 |
Strength Unit | mg/mL; mg/mL |
Pharmaceutical Classes |