NDC product
Camilia Bedtime
NDC 0220-9102 · Boiron
Key facts
| Product NDC | 0220-9102 |
|---|---|
| Proprietary name | Camilia Bedtime |
| Nonproprietary name | MATRICARIA CHAMOMILLA, ARABICA COFFEE BEAN, PHYTOLACCA AMERICANA ROOT, RHEUM OFFICINALE ROOT |
| Substances | PHYTOLACCA AMERICANA ROOT, MATRICARIA CHAMOMILLA, RHEUM OFFICINALE ROOT, ARABICA COFFEE BEAN |
| Dosage form | LIQUID |
| Route | ORAL |
| Labeler | Boiron |
| Product type | HUMAN OTC DRUG |
| Marketing category | UNAPPROVED HOMEOPATHIC |
| Pharmacologic classes | Allergens [CS], Cell-mediated Immunity [PE], Dietary Proteins [CS], Increased Histamine Release [PE], Non-Standardized Food Allergenic Extract [EPC], Non-Standardized Plant Allergenic Extract [EPC] and 2 more |
| Marketing start | Aug 19, 2024 |
| 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: