| Product NDC: | 49789-060 |
| Proprietary Name: | HIS ULC MINT BLUE |
| Non Proprietary Name: | Calcium carbonate |
| Active Ingredient(s): | 350 mg/492mg & nbsp; Calcium carbonate |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, CHEWABLE |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 49789-060 |
| Labeler Name: | SAMSUNG PHARM IND. CO., LTD. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part331 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20121201 |
| Package NDC: | 49789-060-01 |
| Package Description: | 492 mg in 1 BLISTER PACK (49789-060-01) |
| NDC Code | 49789-060-01 |
| Proprietary Name | HIS ULC MINT BLUE |
| Package Description | 492 mg in 1 BLISTER PACK (49789-060-01) |
| Product NDC | 49789-060 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Calcium carbonate |
| Dosage Form Name | TABLET, CHEWABLE |
| Route Name | ORAL |
| Start Marketing Date | 20121201 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | SAMSUNG PHARM IND. CO., LTD. |
| Substance Name | CALCIUM CARBONATE |
| Strength Number | 350 |
| Strength Unit | mg/492mg |
| Pharmaceutical Classes |