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 |