NDC product
Weed Grass Antigens
NDC 44911-0553 · Energique, Inc.
Key facts
| Product NDC | 44911-0553 |
|---|---|
| Proprietary name | Weed Grass Antigens |
| Nonproprietary name | Allium Cepa, Arsenicum Album, Natrum Muriaticum, Nux Vomica, Pulsatilla (Pratensis), Abrotanum (Artemisia Abrotanum), Absinthium, Agrimonia Eupatoria, Flos, Alfalfa, Ambrosia Artemisiaefolia, Arundo Mauritanica and 17 more |
| Substances | ONION, ARSENIC TRIOXIDE, SODIUM CHLORIDE, STRYCHNOS NUX-VOMICA SEED, PULSATILLA PRATENSIS WHOLE, ARTEMISIA ABROTANUM FLOWERING TOP, WORMWOOD, AGRIMONIA EUPATORIA FLOWER, MEDICAGO SATIVA WHOLE, AMBROSIA ARTEMISIIFOLIA WHOLE, ARUNDO PLINIANA ROOT, BAMBUSA BAMBOS LEAF and 17 more |
| 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 7 more |
| Marketing start | Jul 31, 2020 |
| 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: