Product NDC: | 51134-0062 |
Proprietary Name: | Redness reliever |
Non Proprietary Name: | tetrahydrozoline HCl |
Active Ingredient(s): | .5 mg/mL & nbsp; tetrahydrozoline HCl |
Administration Route(s): | OPHTHALMIC |
Dosage Form(s): | LIQUID |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 51134-0062 |
Labeler Name: | Samchundang Pharm. Co., Ltd. |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part349 |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 20100829 |
Package NDC: | 51134-0062-5 |
Package Description: | 1 BOTTLE in 1 BOX (51134-0062-5) > 15 mL in 1 BOTTLE |
NDC Code | 51134-0062-5 |
Proprietary Name | Redness reliever |
Package Description | 1 BOTTLE in 1 BOX (51134-0062-5) > 15 mL in 1 BOTTLE |
Product NDC | 51134-0062 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | tetrahydrozoline HCl |
Dosage Form Name | LIQUID |
Route Name | OPHTHALMIC |
Start Marketing Date | 20100829 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | Samchundang Pharm. Co., Ltd. |
Substance Name | TETRAHYDROZOLINE HYDROCHLORIDE |
Strength Number | .5 |
Strength Unit | mg/mL |
Pharmaceutical Classes |