Product NDC: | 41520-532 |
Proprietary Name: | Advanced relief |
Non Proprietary Name: | dextran 70, polyethylene glycol 400, povidone, tetrahydrozoline HCl |
Active Ingredient(s): | 1; 10; 10; .5 mg/mL; mg/mL; mg/mL; mg/mL & nbsp; dextran 70, polyethylene glycol 400, povidone, tetrahydrozoline HCl |
Administration Route(s): | OPHTHALMIC |
Dosage Form(s): | LIQUID |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 41520-532 |
Labeler Name: | American Sales Company |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part349 |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 20110907 |
Package NDC: | 41520-532-05 |
Package Description: | 1 BOTTLE in 1 BOX (41520-532-05) > 15 mL in 1 BOTTLE |
NDC Code | 41520-532-05 |
Proprietary Name | Advanced relief |
Package Description | 1 BOTTLE in 1 BOX (41520-532-05) > 15 mL in 1 BOTTLE |
Product NDC | 41520-532 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | dextran 70, polyethylene glycol 400, povidone, tetrahydrozoline HCl |
Dosage Form Name | LIQUID |
Route Name | OPHTHALMIC |
Start Marketing Date | 20110907 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | American Sales Company |
Substance Name | DEXTRAN 70; POLYETHYLENE GLYCOL 400; POVIDONE; TETRAHYDROZOLINE HYDROCHLORIDE |
Strength Number | 1; 10; 10; .5 |
Strength Unit | mg/mL; mg/mL; mg/mL; mg/mL |
Pharmaceutical Classes |