Product NDC: | 64809-104 |
Proprietary Name: | Eyesaline Concentrate |
Non Proprietary Name: | Water |
Active Ingredient(s): | 92.2 mL/100mL & nbsp; Water |
Administration Route(s): | OPHTHALMIC |
Dosage Form(s): | LIQUID |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 64809-104 |
Labeler Name: | Sperian Eye & Face Protection Inc. |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part349 |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 20110908 |
Package NDC: | 64809-104-18 |
Package Description: | 2070 mL in 1 BOTTLE, PLASTIC (64809-104-18) |
NDC Code | 64809-104-18 |
Proprietary Name | Eyesaline Concentrate |
Package Description | 2070 mL in 1 BOTTLE, PLASTIC (64809-104-18) |
Product NDC | 64809-104 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Water |
Dosage Form Name | LIQUID |
Route Name | OPHTHALMIC |
Start Marketing Date | 20110908 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | Sperian Eye & Face Protection Inc. |
Substance Name | WATER |
Strength Number | 92.2 |
Strength Unit | mL/100mL |
Pharmaceutical Classes |