Cholestop is a Sublingual Pellet in the Human Otc Drug category. It is labeled and distributed by Homeocare Laboratories. The primary component is Arctium Lappa Whole; Berberis Vulgaris Root Bark; Silybum Marianum Seed; Chelidonium Majus; Cholesterol; Chrysanthellum Indicum Subsp. Afroamericanum; Solidago Canadensis Flowering Top; Taraxacum Palustre Root.
| Product ID | 61727-329_7e59337a-caed-1c5d-e053-2a91aa0a417e |
| NDC | 61727-329 |
| Product Type | Human Otc Drug |
| Proprietary Name | Cholestop |
| Generic Name | Arctium Lappa Whole, Berberis Vulgaris Root Bark, Silybum Marianum Seed, Chelidonium Majus, Cholesterol, Chrysanthellum Indicum Subsp, Afroamericanum, Solidago Canadensis Flowering Top, Taraxacum Palustre Root |
| Dosage Form | Pellet |
| Route of Administration | SUBLINGUAL |
| Marketing Start Date | 2012-06-18 |
| Marketing Category | UNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC |
| Labeler Name | Homeocare Laboratories |
| Substance Name | ARCTIUM LAPPA WHOLE; BERBERIS VULGARIS ROOT BARK; SILYBUM MARIANUM SEED; CHELIDONIUM MAJUS; CHOLESTEROL; CHRYSANTHELLUM INDICUM SUBSP. AFROAMERICANUM; SOLIDAGO CANADENSIS FLOWERING TOP; TARAXACUM PALUSTRE ROOT |
| Active Ingredient Strength | 4 [hp_X]/4g; [hp_X]/4g; [hp_X]/4g; [hp_X]/4g; [hp_C]/4g; [hp_X]/4g; [hp_X]/4g; [hp_X]/4g |
| NDC Exclude Flag | N |
| Listing Certified Through | 2020-12-31 |
| Marketing Start Date | 2012-06-18 |
| NDC Exclude Flag | N |
| Sample Package? | N |
| Marketing Category | unapproved homeopathic |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2012-06-18 |
| Ingredient | Strength |
|---|---|
| ARCTIUM LAPPA WHOLE | 4 [hp_X]/4g |
| SPL SET ID: | 1eb44103-03d3-442e-bcf0-3d360ff3096a |
| Manufacturer | |
| UNII | |
| UPC Code |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() CHOLESTOP 73834604 1619384 Dead/Cancelled |
NATURE'S WAY PRODUCTS, INC. 1989-10-30 |