| 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 |