| 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 |