| Product NDC: | 51596-005 |
| Proprietary Name: | Heartburn Relief to Go |
| Non Proprietary Name: | Calcium carbonate |
| Active Ingredient(s): | 1000 mg/1 & nbsp; Calcium carbonate |
| Administration Route(s): | ORAL |
| Dosage Form(s): | POWDER |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 51596-005 |
| Labeler Name: | Breakthrough Products Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part331 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20110901 |
| Package NDC: | 51596-005-24 |
| Package Description: | 24 POUCH in 1 BOX (51596-005-24) > 1 POWDER in 1 POUCH (51596-005-01) |
| NDC Code | 51596-005-24 |
| Proprietary Name | Heartburn Relief to Go |
| Package Description | 24 POUCH in 1 BOX (51596-005-24) > 1 POWDER in 1 POUCH (51596-005-01) |
| Product NDC | 51596-005 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Calcium carbonate |
| Dosage Form Name | POWDER |
| Route Name | ORAL |
| Start Marketing Date | 20110901 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Breakthrough Products Inc. |
| Substance Name | CALCIUM CARBONATE |
| Strength Number | 1000 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |