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OCUFLUSH
OCUFLUSH - 64108-090-16 - (WATER)
Drug Information of OCUFLUSH
| Product NDC: | 64108-090 |
| Proprietary Name: | OCUFLUSH |
| Non Proprietary Name: | WATER |
| Active Ingredient(s): | 99.01 mL/100mL & nbsp; WATER |
| Administration Route(s): | OPHTHALMIC |
| Dosage Form(s): | LIQUID |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of OCUFLUSH
| Product NDC: | 64108-090 |
| Labeler Name: | Optics Laboratory, Inc |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part349 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20121001 |
Package Information of OCUFLUSH
| Package NDC: | 64108-090-16 |
| Package Description: | 473 mL in 1 BOTTLE (64108-090-16) |
NDC Information of OCUFLUSH
| NDC Code | 64108-090-16 |
| Proprietary Name | OCUFLUSH |
| Package Description | 473 mL in 1 BOTTLE (64108-090-16) |
| Product NDC | 64108-090 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | WATER |
| Dosage Form Name | LIQUID |
| Route Name | OPHTHALMIC |
| Start Marketing Date | 20121001 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Optics Laboratory, Inc |
| Substance Name | WATER |
| Strength Number | 99.01 |
| Strength Unit | mL/100mL |
| Pharmaceutical Classes |
