NDC product
Upper Resp HP
NDC 44911-0595 · Energique, Inc.
Key facts
| Product NDC | 44911-0595 |
|---|---|
| Proprietary name | Upper Resp HP |
| Nonproprietary name | Carbo Vegetabilis, Cuprum Metallicum, Drosera (Rotundifolia), Hepar Sulphuris Calcareum, Ipecacuanha, Lachesis Mutus, Lobelia Inflata, Phosphorus, Pulsatilla (Pratensis), Rumex Crispus, Spongia Tosta |
| Substances | ACTIVATED CHARCOAL, COPPER, DROSERA ROTUNDIFOLIA WHOLE, CALCIUM SULFIDE, IPECAC, LACHESIS MUTA VENOM, LOBELIA INFLATA WHOLE, PHOSPHORUS, PULSATILLA PRATENSIS WHOLE, RUMEX CRISPUS ROOT, SPONGIA OFFICINALIS SKELETON, ROASTED |
| Dosage form | LIQUID |
| Route | ORAL |
| Labeler | Energique, Inc. |
| Product type | HUMAN OTC DRUG |
| Marketing category | UNAPPROVED HOMEOPATHIC |
| Pharmacologic classes | Copper [CS], Copper-containing Intrauterine Device [EPC], Decreased Embryonic Implantation [PE], Decreased Sperm Motility [PE], Inhibit Ovum Fertilization [PE] |
| Marketing start | Jan 4, 2021 |
| 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: