| Product NDC: | 49873-044 |
| Proprietary Name: | Sato Clear |
| Non Proprietary Name: | NAPHAZOLINE HYDROCHLORIDE |
| Active Ingredient(s): | 12 mg/100mL & nbsp; NAPHAZOLINE HYDROCHLORIDE |
| Administration Route(s): | OPHTHALMIC |
| Dosage Form(s): | SOLUTION/ DROPS |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 49873-044 |
| Labeler Name: | Sato Pharmaceutical Co., Ltd. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part349 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 19890531 |
| Package NDC: | 49873-044-01 |
| Package Description: | 1 BOTTLE, PLASTIC in 1 CARTON (49873-044-01) > 15 mL in 1 BOTTLE, PLASTIC |
| NDC Code | 49873-044-01 |
| Proprietary Name | Sato Clear |
| Package Description | 1 BOTTLE, PLASTIC in 1 CARTON (49873-044-01) > 15 mL in 1 BOTTLE, PLASTIC |
| Product NDC | 49873-044 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | NAPHAZOLINE HYDROCHLORIDE |
| Dosage Form Name | SOLUTION/ DROPS |
| Route Name | OPHTHALMIC |
| Start Marketing Date | 19890531 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Sato Pharmaceutical Co., Ltd. |
| Substance Name | NAPHAZOLINE HYDROCHLORIDE |
| Strength Number | 12 |
| Strength Unit | mg/100mL |
| Pharmaceutical Classes |