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Rohto Relief
Rohto Relief - 66613-8149-1 - (hypromellose, tetrahydrozoline HCl, zinc sulfate)
Drug Information of Rohto Relief
| Product NDC: | 66613-8149 |
| Proprietary Name: | Rohto Relief |
| Non Proprietary Name: | hypromellose, tetrahydrozoline HCl, zinc sulfate |
| Active Ingredient(s): | 2; .5; 2.5 mg/mL; mg/mL; mg/mL & nbsp; hypromellose, tetrahydrozoline HCl, zinc sulfate |
| Administration Route(s): | OPHTHALMIC |
| Dosage Form(s): | LIQUID |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Rohto Relief
| Product NDC: | 66613-8149 |
| Labeler Name: | Rohto Pharmaceutical Co Ltd |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part349 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20111201 |
Package Information of Rohto Relief
| Package NDC: | 66613-8149-1 |
| Package Description: | 1 BOTTLE in 1 CARTON (66613-8149-1) > 13 mL in 1 BOTTLE |
NDC Information of Rohto Relief
| NDC Code | 66613-8149-1 |
| Proprietary Name | Rohto Relief |
| Package Description | 1 BOTTLE in 1 CARTON (66613-8149-1) > 13 mL in 1 BOTTLE |
| Product NDC | 66613-8149 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | hypromellose, tetrahydrozoline HCl, zinc sulfate |
| Dosage Form Name | LIQUID |
| Route Name | OPHTHALMIC |
| Start Marketing Date | 20111201 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Rohto Pharmaceutical Co Ltd |
| Substance Name | HYPROMELLOSES; TETRAHYDROZOLINE HYDROCHLORIDE; ZINC SULFATE |
| Strength Number | 2; .5; 2.5 |
| Strength Unit | mg/mL; mg/mL; mg/mL |
| Pharmaceutical Classes |
