NDC product

Appetrol 20

NDC 87115-0001 · Carbalor LLC

Key facts

Product NDC 87115-0001
Proprietary name Appetrol 20
Nonproprietary name Fucus Vesiculosus, Chelidonium Majus, Kali Phosphoricum, Lycopodium Clavatum, Natrum Muriaticum, Quercus Glandium Spiritus, Quercus Robur, Nux Vomica, Phytolacca Decandra, Ornithogalum Umbellatum, Agnus Castus, Berberis Aquifolium and 14 more
Substances FUCUS VESICULOSUS, CHELIDONIUM MAJUS WHOLE, DIBASIC POTASSIUM PHOSPHATE, LYCOPODIUM CLAVATUM SPORE, SODIUM CHLORIDE, QUERCUS ROBUR NUT, QUERCUS ROBUR TWIG BARK, STRYCHNOS NUX-VOMICA SEED, PHYTOLACCA AMERICANA ROOT, ORNITHOGALUM UMBELLATUM WHOLE, CHASTE TREE FRUIT, BERBERIS AQUIFOLIUM ROOT BARK and 13 more
Dosage form LIQUID
Route ORAL
Labeler Carbalor LLC
Product type HUMAN OTC DRUG
Marketing category UNAPPROVED HOMEOPATHIC
Pharmacologic classes Allergens [CS], Calculi Dissolution Agent [EPC], Cell-mediated Immunity [PE], Increased Histamine Release [PE], Increased IgG Production [PE], Increased Large Intestinal Motility [PE] and 9 more
Marketing start Mar 12, 2026
Listing certified through Dec 31, 2027

At a glance

  • 1–9 Package NDCs

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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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