NDC product
CHESTAL COUGH AND MUCUS
NDC 0220-9115 · Boiron
Key facts
| Product NDC | 0220-9115 |
|---|---|
| Proprietary name | CHESTAL COUGH AND MUCUS |
| Nonproprietary name | ANTIMONY POTASSIUM TARTRATE, BRYONIA ALBA ROOT, PROTORTONIA CACTI, DROSERA ROTUNDIFOLIA, IPECAC, PULSATILLA VULGARIS WHOLE, RUMEX CRISPUS ROOT, SPONGIA OFFICINALIS SKELETON, ROASTED, LOBARIA PULMONARIA |
| Substances | SPONGIA OFFICINALIS SKELETON, ROASTED, IPECAC, RUMEX CRISPUS ROOT, LOBARIA PULMONARIA, PROTORTONIA CACTI, DROSERA ROTUNDIFOLIA, PULSATILLA VULGARIS WHOLE, ANTIMONY POTASSIUM TARTRATE, BRYONIA ALBA ROOT |
| Dosage form | TABLET |
| Route | ORAL |
| Labeler | Boiron |
| Product type | HUMAN OTC DRUG |
| Marketing category | UNAPPROVED HOMEOPATHIC |
| Marketing start | Mar 20, 2026 |
| 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: