NDC product
Sniffles
NDC 55714-1529 · Newton Laboratories, Inc.
Key facts
| Product NDC | 55714-1529 |
|---|---|
| Proprietary name | Sniffles |
| Nonproprietary name | Echinacea, Aconitum napellus, Aralia quinquefolia, Arsenicum album, Bryonia, Euphrasia officinalis, Gaultheria procumbens, Gelsemium sempervirens, Histaminum hydrochloricum, Hydrastis canadensis, Kali bichromicum, Lycopodium clavatum and 10 more |
| Substances | ECHINACEA, UNSPECIFIED, STRYCHNOS NUX-VOMICA SEED, AMERICAN GINSENG, ARSENIC TRIOXIDE, BRYONIA ALBA ROOT, EUPHRASIA STRICTA, GAULTHERIA PROCUMBENS TOP, GELSEMIUM SEMPERVIRENS ROOT, HISTAMINE DIHYDROCHLORIDE, GOLDENSEAL, POTASSIUM DICHROMATE, LYCOPODIUM CLAVATUM SPORE and 11 more |
| Dosage form | LIQUID |
| Route | ORAL |
| Labeler | Newton Laboratories, 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 3 more |
| Marketing start | Jan 1, 2019 |
| 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: