NDC product
LY-CO
NDC 58048-0006 · Bhp Holdings, Inc.
Key facts
| Product NDC | 58048-0006 |
|---|---|
| Proprietary name | LY-CO |
| Nonproprietary name | Angelica Archangelica, Kali Muriaticum, Yucca Filamentosa, Cartilago Suis, Phytolacca Decandra, Hydrastis Canadensis, Rhus Tox, Causticum, Magnesia Phosphorica, Manganum Metallicum, Oxalicum Acidum, Arnica Montana and 7 more |
| Substances | ANGELICA ARCHANGELICA ROOT, POTASSIUM CHLORIDE, YUCCA FILAMENTOSA WHOLE, SUS SCROFA CARTILAGE, PHYTOLACCA AMERICANA ROOT, GOLDENSEAL, TOXICODENDRON PUBESCENS LEAF, CAUSTICUM, MAGNESIUM PHOSPHATE, DIBASIC TRIHYDRATE, MANGANESE, OXALIC ACID DIHYDRATE, ARNICA MONTANA WHOLE and 7 more |
| Dosage form | LIQUID |
| Route | ORAL |
| Labeler | Bhp Holdings, Inc. |
| Product type | HUMAN OTC DRUG |
| Marketing category | UNAPPROVED HOMEOPATHIC |
| Pharmacologic classes | Acidifying Activity [MoA], Anti-coagulant [EPC], Calcium Chelating Activity [MoA], Calculi Dissolution Agent [EPC], Decreased Coagulation Factor Activity [PE], Increased Large Intestinal Motility [PE] and 8 more |
| Marketing start | Jun 1, 2023 |
| Listing certified through | Dec 31, 2027 |
At a glance
- 1–9 Package NDCs
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About National Drug Codes (NDC)
The National Drug Code (NDC) is the FDA's product identifier for drugs; the product NDC identifies the labeler and product, and each package adds a package code.
Source: U.S. Food and Drug Administration (FDA), National Drug Code Directory · Source date: