NDC product
Cold HP
NDC 44911-0089 · Energique, Inc.
Key facts
| Product NDC | 44911-0089 |
|---|---|
| Proprietary name | Cold HP |
| Nonproprietary name | Aconitum Napellus, Allium Cepa, Eupatorium Perfoliatum, Ferrum Phosphoricum, Gelsemium Sempervirens, Kali Bichromicum, Mercurius Solubilis, Nux Vomica, Pulsatilla (Vulgaris) |
| Substances | ACONITUM NAPELLUS WHOLE, ONION, EUPATORIUM PERFOLIATUM FLOWERING TOP, FERRUM PHOSPHORICUM, GELSEMIUM SEMPERVIRENS ROOT, POTASSIUM DICHROMATE, MERCURIUS SOLUBILIS, STRYCHNOS NUX-VOMICA SEED, PULSATILLA VULGARIS |
| Dosage form | LIQUID |
| Route | ORAL |
| Labeler | Energique, Inc. |
| Product type | HUMAN OTC DRUG |
| Marketing category | UNAPPROVED HOMEOPATHIC |
| Pharmacologic classes | Allergens [CS], Cell-mediated Immunity [PE], Dietary Proteins [CS], Increased Histamine Release [PE], Increased IgG Production [PE], Non-Standardized Food Allergenic Extract [EPC] and 4 more |
| Marketing start | Aug 21, 2013 |
| Listing certified through | Dec 31, 2026 |
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: