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SHOPKO RELIEF
SHOPKO RELIEF - 11716-0460-1 - (TETRAHYDROZOLINE HYDROCHLORIDE AND ZINC SULFATE)
Drug Information of SHOPKO RELIEF
| Product NDC: | 11716-0460 |
| Proprietary Name: | SHOPKO RELIEF |
| Non Proprietary Name: | TETRAHYDROZOLINE HYDROCHLORIDE AND ZINC SULFATE |
| Active Ingredient(s): | .5; 2.5 mg/mL; mg/mL & nbsp; TETRAHYDROZOLINE HYDROCHLORIDE AND ZINC SULFATE |
| Administration Route(s): | OPHTHALMIC |
| Dosage Form(s): | SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of SHOPKO RELIEF
| Product NDC: | 11716-0460 |
| Labeler Name: | HANLIM PHARM. CO., LTD. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part349 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20101008 |
Package Information of SHOPKO RELIEF
| Package NDC: | 11716-0460-1 |
| Package Description: | 1 BOTTLE in 1 CARTON (11716-0460-1) > 15 mL in 1 BOTTLE |
NDC Information of SHOPKO RELIEF
| NDC Code | 11716-0460-1 |
| Proprietary Name | SHOPKO RELIEF |
| Package Description | 1 BOTTLE in 1 CARTON (11716-0460-1) > 15 mL in 1 BOTTLE |
| Product NDC | 11716-0460 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | TETRAHYDROZOLINE HYDROCHLORIDE AND ZINC SULFATE |
| Dosage Form Name | SOLUTION |
| Route Name | OPHTHALMIC |
| Start Marketing Date | 20101008 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | HANLIM PHARM. CO., LTD. |
| Substance Name | TETRAHYDROZOLINE HYDROCHLORIDE; ZINC SULFATE |
| Strength Number | .5; 2.5 |
| Strength Unit | mg/mL; mg/mL |
| Pharmaceutical Classes |
