| Product NDC: | 24286-1537 |
| Proprietary Name: | De La Cruz Sodium Bicarbonate Antacid |
| Non Proprietary Name: | SODIUM BICARBONATE |
| Active Ingredient(s): | 2.5 g/2.5g & nbsp; SODIUM BICARBONATE |
| Administration Route(s): | ORAL |
| Dosage Form(s): | POWDER |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 24286-1537 |
| Labeler Name: | DLC Laboratories, Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part331 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20110523 |
| Package NDC: | 24286-1537-7 |
| Package Description: | 113 g in 1 BOTTLE (24286-1537-7) |
| NDC Code | 24286-1537-7 |
| Proprietary Name | De La Cruz Sodium Bicarbonate Antacid |
| Package Description | 113 g in 1 BOTTLE (24286-1537-7) |
| Product NDC | 24286-1537 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | SODIUM BICARBONATE |
| Dosage Form Name | POWDER |
| Route Name | ORAL |
| Start Marketing Date | 20110523 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | DLC Laboratories, Inc. |
| Substance Name | SODIUM BICARBONATE |
| Strength Number | 2.5 |
| Strength Unit | g/2.5g |
| Pharmaceutical Classes |