Product NDC: | 49873-501 |
Proprietary Name: | Optic Splash |
Non Proprietary Name: | naphazoline hydrochloride, glycerin |
Active Ingredient(s): | 200; 20 mg/100mL; mg/100mL & nbsp; naphazoline hydrochloride, glycerin |
Administration Route(s): | OPHTHALMIC |
Dosage Form(s): | SOLUTION/ DROPS |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 49873-501 |
Labeler Name: | Sato Pharmaceutical, Co., Ltd. |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part349 |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 20080122 |
Package NDC: | 49873-501-01 |
Package Description: | 1 BOTTLE in 1 CARTON (49873-501-01) > 15 mL in 1 BOTTLE |
NDC Code | 49873-501-01 |
Proprietary Name | Optic Splash |
Package Description | 1 BOTTLE in 1 CARTON (49873-501-01) > 15 mL in 1 BOTTLE |
Product NDC | 49873-501 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | naphazoline hydrochloride, glycerin |
Dosage Form Name | SOLUTION/ DROPS |
Route Name | OPHTHALMIC |
Start Marketing Date | 20080122 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | Sato Pharmaceutical, Co., Ltd. |
Substance Name | GLYCERIN; NAPHAZOLINE HYDROCHLORIDE |
Strength Number | 200; 20 |
Strength Unit | mg/100mL; mg/100mL |
Pharmaceutical Classes |