| 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 |