NDC product

Prostate

NDC 55714-2503 · Newton Laboratories, Inc.

Key facts

Product NDC 55714-2503
Proprietary name Prostate
Nonproprietary name Thyroidinum, Baryta carb., Berber. vulg., Bryonia, Calc. carb., Cinchona, Conium, Digitalis, Ferrum picricum, Hydrastis, Iodium, Lycopodium and 11 more
Substances ECHINACEA, UNSPECIFIED, SAW PALMETTO, SELENIUM, DELPHINIUM STAPHISAGRIA SEED, THUJA OCCIDENTALIS LEAFY TWIG, TRIFOLIUM PRATENSE FLOWER, ARCTIUM LAPPA ROOT, SOLIDAGO VIRGAUREA FLOWERING TOP, STRYCHNOS NUX-VOMICA SEED, CHONDRODENDRON TOMENTOSUM ROOT, IODINE, THYROID, UNSPECIFIED 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], Increased Histamine Release [PE], Increased IgG Production [PE], Iron [CS], Non-Standardized Plant Allergenic Extract [EPC] and 5 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:

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