Product NDC: | 65923-555 |
Proprietary Name: | FAMILY CARE LUBRICANT SINGLE USE EYE |
Non Proprietary Name: | CARBOXYMETHYLCELLULOSE SODIUM |
Active Ingredient(s): | 5 mg/mL & nbsp; CARBOXYMETHYLCELLULOSE SODIUM |
Administration Route(s): | OPHTHALMIC |
Dosage Form(s): | SOLUTION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 65923-555 |
Labeler Name: | UNITED EXCHANGE CORP |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part349 |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 20130228 |
Package NDC: | 65923-555-02 |
Package Description: | 5 VIAL, SINGLE-USE in 1 CARTON (65923-555-02) > .8 mL in 1 VIAL, SINGLE-USE |
NDC Code | 65923-555-02 |
Proprietary Name | FAMILY CARE LUBRICANT SINGLE USE EYE |
Package Description | 5 VIAL, SINGLE-USE in 1 CARTON (65923-555-02) > .8 mL in 1 VIAL, SINGLE-USE |
Product NDC | 65923-555 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | CARBOXYMETHYLCELLULOSE SODIUM |
Dosage Form Name | SOLUTION |
Route Name | OPHTHALMIC |
Start Marketing Date | 20130228 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | UNITED EXCHANGE CORP |
Substance Name | CARBOXYMETHYLCELLULOSE SODIUM |
Strength Number | 5 |
Strength Unit | mg/mL |
Pharmaceutical Classes |