Product NDC: | 16995-001 |
Proprietary Name: | FLORIL REDNESS RELIEF |
Non Proprietary Name: | NAPHAZOLINE HYDROCHLORIDE |
Active Ingredient(s): | 3; 2 mg/10mL; mg/mL & nbsp; NAPHAZOLINE HYDROCHLORIDE |
Administration Route(s): | OPHTHALMIC |
Dosage Form(s): | SOLUTION/ DROPS |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 16995-001 |
Labeler Name: | VITALINE S.A.C. |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part349 |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 20051110 |
Package NDC: | 16995-001-03 |
Package Description: | 15 mL in 1 BOTTLE, DROPPER (16995-001-03) |
NDC Code | 16995-001-03 |
Proprietary Name | FLORIL REDNESS RELIEF |
Package Description | 15 mL in 1 BOTTLE, DROPPER (16995-001-03) |
Product NDC | 16995-001 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | NAPHAZOLINE HYDROCHLORIDE |
Dosage Form Name | SOLUTION/ DROPS |
Route Name | OPHTHALMIC |
Start Marketing Date | 20051110 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | VITALINE S.A.C. |
Substance Name | NAPHAZOLINE HYDROCHLORIDE; POLYSORBATE 20 |
Strength Number | 3; 2 |
Strength Unit | mg/10mL; mg/mL |
Pharmaceutical Classes |