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REFRESH PLUS
REFRESH PLUS - 0023-0403-70 - (carboxymethylcellulose sodium)
Drug Information of REFRESH PLUS
| Product NDC: | 0023-0403 |
| Proprietary Name: | REFRESH PLUS |
| Non Proprietary Name: | carboxymethylcellulose sodium |
| Active Ingredient(s): | 5 mg/mL & nbsp; carboxymethylcellulose sodium |
| Administration Route(s): | OPHTHALMIC |
| Dosage Form(s): | SOLUTION/ DROPS |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of REFRESH PLUS
| Product NDC: | 0023-0403 |
| Labeler Name: | Allergan, Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part349 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 19961009 |
Package Information of REFRESH PLUS
| Package NDC: | 0023-0403-70 |
| Package Description: | 70 VIAL, SINGLE-USE in 1 CARTON (0023-0403-70) > .4 mL in 1 VIAL, SINGLE-USE |
NDC Information of REFRESH PLUS
| NDC Code | 0023-0403-70 |
| Proprietary Name | REFRESH PLUS |
| Package Description | 70 VIAL, SINGLE-USE in 1 CARTON (0023-0403-70) > .4 mL in 1 VIAL, SINGLE-USE |
| Product NDC | 0023-0403 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | carboxymethylcellulose sodium |
| Dosage Form Name | SOLUTION/ DROPS |
| Route Name | OPHTHALMIC |
| Start Marketing Date | 19961009 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Allergan, Inc. |
| Substance Name | CARBOXYMETHYLCELLULOSE SODIUM |
| Strength Number | 5 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes |
