NDC product
Food Additives
NDC 55714-2544 · Newton Laboratories, Inc.
Key facts
| Product NDC | 55714-2544 |
|---|---|
| Proprietary name | Food Additives |
| Nonproprietary name | Iris versicolor, Solidago virgaurea, Aconitum napellus, Agaricus muscarius, Allium cepa, Allium sativum, Antimonium crudum, Arsenicum album, Baptisia tinctoria, Bovista, Caffeinum, Capsicum annuum and 16 more |
| Substances | EGG SHELL, COOKED, LYCOPODIUM CLAVATUM SPORE, RHODODENDRON TOMENTOSUM LEAFY TWIG, ASCORBIC ACID, BLACK MUSTARD SEED, SOLANUM NIGRUM WHOLE, ANACARDIUM OCCIDENTALE FRUIT, SOLANUM LYCOPERSICUM, SODIUM NITRITE, SODIUM CHLORIDE, ANEMONE PULSATILLA, TOXICODENDRON PUBESCENS LEAF and 40 more |
| Dosage form | LIQUID |
| Route | ORAL |
| Labeler | Newton Laboratories, Inc. |
| Product type | HUMAN OTC DRUG |
| Marketing category | UNAPPROVED HOMEOPATHIC |
| Pharmacologic classes | Allergens [CS], Ascorbic Acid [CS], Cell-mediated Immunity [PE], Central Nervous System Stimulant [EPC], Central Nervous System Stimulation [PE], Dietary Proteins [CS] and 13 more |
| Marketing start | Jul 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: