| Product NDC: | 55651-024 |
| Proprietary Name: | Eye Drops AC |
| Non Proprietary Name: | Tetrahydrozoline hydrochloride, Zinc sulfate |
| Active Ingredient(s): | .5; 2.5 mg/mL; mg/mL & nbsp; Tetrahydrozoline hydrochloride, Zinc sulfate |
| Administration Route(s): | OPHTHALMIC |
| Dosage Form(s): | SOLUTION/ DROPS |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 55651-024 |
| Labeler Name: | KC Pharmaceuticals, Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part349 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20031023 |
| Package NDC: | 55651-024-01 |
| Package Description: | 1 BOTTLE, DROPPER in 1 CARTON (55651-024-01) > 15 mL in 1 BOTTLE, DROPPER |
| NDC Code | 55651-024-01 |
| Proprietary Name | Eye Drops AC |
| Package Description | 1 BOTTLE, DROPPER in 1 CARTON (55651-024-01) > 15 mL in 1 BOTTLE, DROPPER |
| Product NDC | 55651-024 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Tetrahydrozoline hydrochloride, Zinc sulfate |
| Dosage Form Name | SOLUTION/ DROPS |
| Route Name | OPHTHALMIC |
| Start Marketing Date | 20031023 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | KC Pharmaceuticals, Inc. |
| Substance Name | TETRAHYDROZOLINE HYDROCHLORIDE; ZINC SULFATE |
| Strength Number | .5; 2.5 |
| Strength Unit | mg/mL; mg/mL |
| Pharmaceutical Classes |