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Ocufresh
Ocufresh - 62622-201-12 - (Eyewash)
Drug Information of Ocufresh
| Product NDC: | 62622-201 |
| Proprietary Name: | Ocufresh |
| Non Proprietary Name: | Eyewash |
| Active Ingredient(s): | 99.1 mL/100mL & nbsp; Eyewash |
| Administration Route(s): | OPHTHALMIC |
| Dosage Form(s): | LIQUID |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Ocufresh
| Product NDC: | 62622-201 |
| Labeler Name: | Taiwan Biotech Co, Ltd |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part349 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 19910401 |
Package Information of Ocufresh
| Package NDC: | 62622-201-12 |
| Package Description: | 6 DOSE PACK in 1 BOX (62622-201-12) > 20 mL in 1 DOSE PACK (62622-201-11) |
NDC Information of Ocufresh
| NDC Code | 62622-201-12 |
| Proprietary Name | Ocufresh |
| Package Description | 6 DOSE PACK in 1 BOX (62622-201-12) > 20 mL in 1 DOSE PACK (62622-201-11) |
| Product NDC | 62622-201 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Eyewash |
| Dosage Form Name | LIQUID |
| Route Name | OPHTHALMIC |
| Start Marketing Date | 19910401 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Taiwan Biotech Co, Ltd |
| Substance Name | WATER |
| Strength Number | 99.1 |
| Strength Unit | mL/100mL |
| Pharmaceutical Classes |
