Product NDC: | 50383-018 |
Proprietary Name: | Eye Wash |
Non Proprietary Name: | Eye Wash |
Active Ingredient(s): | 980 mg/mL & nbsp; Eye Wash |
Administration Route(s): | AURICULAR (OTIC) |
Dosage Form(s): | SOLUTION/ DROPS |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 50383-018 |
Labeler Name: | Hi-Tech Pharmacal Co., Inc. |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | |
Marketing Category: | UNAPPROVED OTHER |
Start Marketing Date: | 19970106 |
Package NDC: | 50383-018-04 |
Package Description: | 1 BOTTLE in 1 CARTON (50383-018-04) > 118 mL in 1 BOTTLE |
NDC Code | 50383-018-04 |
Proprietary Name | Eye Wash |
Package Description | 1 BOTTLE in 1 CARTON (50383-018-04) > 118 mL in 1 BOTTLE |
Product NDC | 50383-018 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Eye Wash |
Dosage Form Name | SOLUTION/ DROPS |
Route Name | AURICULAR (OTIC) |
Start Marketing Date | 19970106 |
Marketing Category Name | UNAPPROVED OTHER |
Labeler Name | Hi-Tech Pharmacal Co., Inc. |
Substance Name | WATER |
Strength Number | 980 |
Strength Unit | mg/mL |
Pharmaceutical Classes |