| Product NDC: | 61727-304 |
| Proprietary Name: | Constipation Relief |
| Non Proprietary Name: | ALUMINUM OXIDE,BRYONIA ALBA ROOT,SODIUM CHLORIDE,GRAPHITE,SILICON DIOXIDE. |
| Active Ingredient(s): | 10; 8; 10; 10; 8 [hp_X]/4g; [hp_X]/4g; [hp_X]/4g; [hp_X]/4g; [hp_X]/4g & nbsp; ALUMINUM OXIDE,BRYONIA ALBA ROOT,SODIUM CHLORIDE,GRAPHITE,SILICON DIOXIDE. |
| Administration Route(s): | SUBLINGUAL |
| Dosage Form(s): | PELLET |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 61727-304 |
| Labeler Name: | Homeocare Laboratories |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED HOMEOPATHIC |
| Start Marketing Date: | 20120705 |
| Package NDC: | 61727-304-21 |
| Package Description: | 4 g in 1 TUBE (61727-304-21) |
| NDC Code | 61727-304-21 |
| Proprietary Name | Constipation Relief |
| Package Description | 4 g in 1 TUBE (61727-304-21) |
| Product NDC | 61727-304 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | ALUMINUM OXIDE,BRYONIA ALBA ROOT,SODIUM CHLORIDE,GRAPHITE,SILICON DIOXIDE. |
| Dosage Form Name | PELLET |
| Route Name | SUBLINGUAL |
| Start Marketing Date | 20120705 |
| Marketing Category Name | UNAPPROVED HOMEOPATHIC |
| Labeler Name | Homeocare Laboratories |
| Substance Name | ALUMINUM OXIDE; BRYONIA ALBA ROOT; GRAPHITE; SILICON DIOXIDE; SODIUM CHLORIDE |
| Strength Number | 10; 8; 10; 10; 8 |
| Strength Unit | [hp_X]/4g; [hp_X]/4g; [hp_X]/4g; [hp_X]/4g; [hp_X]/4g |
| Pharmaceutical Classes |