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FLORIL REDNESS RELIEF
FLORIL REDNESS RELIEF - 16995-001-01 - (NAPHAZOLINE HYDROCHLORIDE)
Drug Information of FLORIL REDNESS RELIEF
| 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) |
Labeler Information of FLORIL REDNESS RELIEF
| 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 Information of FLORIL REDNESS RELIEF
| Package NDC: | 16995-001-01 |
| Package Description: | 3 mL in 1 BOTTLE, DROPPER (16995-001-01) |
NDC Information of FLORIL REDNESS RELIEF
| NDC Code | 16995-001-01 |
| Proprietary Name | FLORIL REDNESS RELIEF |
| Package Description | 3 mL in 1 BOTTLE, DROPPER (16995-001-01) |
| 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 |
