Cinnamomum

NDC 37662-0335 · Hahnemann Laboratories, INC.

Generic nameCinnamomum

Dosage formPELLET

RouteORAL

Active ingredient(s)CINNAMON

Strength1 [hp_M]/1

Pharmacologic classAllergens [CS], Cell-mediated Immunity [PE], Dietary Proteins [CS], Food Additives [CS], Increased Histamine Release [PE], Non-Standardized Food Allergenic Extract [EPC]

Marketing categoryUNAPPROVED HOMEOPATHIC

Packages

37662-0335-1 — 200 PELLET in 1 VIAL, GLASS (37662-0335-1)

37662-0335-2 — 500 PELLET in 1 VIAL, GLASS (37662-0335-2)

37662-0335-3 — 3000 PELLET in 1 BOTTLE, GLASS (37662-0335-3)

37662-0335-4 — 10000 PELLET in 1 BOTTLE, GLASS (37662-0335-4)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

0220-1343 — CINNAMON, 0220-1406 — CINNAMON, 0268-6123 — CINNAMOMUM VERUM, 22840-5717 — Cinnamomum verum, 37662-0329 — Cinnamomum, 37662-0330 — Cinnamomum, 37662-0331 — Cinnamomum, 37662-0332 — Cinnamomum, 37662-0333 — Cinnamomum, 37662-0334 — Cinnamomum, 37662-2758 — Cinnamomum, 37662-2759 — Cinnamomum, 37662-2760 — Cinnamomum, 37662-2761 — Cinnamomum, 37662-2762 — Cinnamomum, 37662-2763 — Cinnamomum, 37662-2764 — Cinnamomum, 37662-2765 — Cinnamomum, 43742-1650 — Cinnamomum, Gentiana Lutea, Syzygium Jambolanum, Argentum Nitricum, Colchicum Autumnale, Colostrum (Bovine), Copper Gluconate, Lappa Major, Lycopodium Clavatum, Magnesium Gluconicum, Manganese Gluconate, Pancreas Suis, Potassium Gluconate, Rumex Crispus, Stomach (Suis), Aurum Metallicum, Calcarea Carbonica, Carbo Vegetabilis, Intestine (Suis), Malus Pumila, Flos, Nitricum Acidum, Prunus Cerasifera, Flos, Rock Water, Schrophularia Nodosa, Fagus Sylvatica, Flos, 43742-1665 — Arnica Montana, Cinnamomum, Dulcamara, Funiculus Umbilicalis Suis, Nadidum, Natrum Oxalaceticum, Pantothenic Acid, Placenta Totalis Suis, Sanguinaria Canadensis, Sulphur, Piper Nigrum, Alpha-Lipoicum Acidum, Cartilago Suis, Rhus Tox, Silicea, Symphytum Officinale, Thuja Occidentalis, Apiolum, +32 more

From the FDA National Drug Code Directory, retrieved August 24, 2026. Product listings are submitted by labelers; FDA does not verify them.