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REFRESH LIQUIGEL
REFRESH LIQUIGEL - 0023-9205-15 - (Carboxymethylcellulose sodium)
Drug Information of REFRESH LIQUIGEL
| Product NDC: | 0023-9205 |
| Proprietary Name: | REFRESH LIQUIGEL |
| Non Proprietary Name: | Carboxymethylcellulose sodium |
| Active Ingredient(s): | 10 mg/mL & nbsp; Carboxymethylcellulose sodium |
| Administration Route(s): | OPHTHALMIC |
| Dosage Form(s): | SOLUTION/ DROPS |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of REFRESH LIQUIGEL
| Product NDC: | 0023-9205 |
| Labeler Name: | Allergan, Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part349 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20011004 |
Package Information of REFRESH LIQUIGEL
| Package NDC: | 0023-9205-15 |
| Package Description: | 1 BOTTLE, DROPPER in 1 CARTON (0023-9205-15) > 15 mL in 1 BOTTLE, DROPPER |
NDC Information of REFRESH LIQUIGEL
| NDC Code | 0023-9205-15 |
| Proprietary Name | REFRESH LIQUIGEL |
| Package Description | 1 BOTTLE, DROPPER in 1 CARTON (0023-9205-15) > 15 mL in 1 BOTTLE, DROPPER |
| Product NDC | 0023-9205 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Carboxymethylcellulose sodium |
| Dosage Form Name | SOLUTION/ DROPS |
| Route Name | OPHTHALMIC |
| Start Marketing Date | 20011004 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Allergan, Inc. |
| Substance Name | CARBOXYMETHYLCELLULOSE SODIUM |
| Strength Number | 10 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes |
