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Eucalyptus Globulus

NDC 37662-0686 · Hahnemann Laboratories, INC.

Generic nameEucalyptus Globulus
Dosage formPELLET
RouteORAL
Active ingredient(s)EUCALYPTUS GLOBULUS LEAF
Strength500 [hp_C]/1
Marketing categoryUNAPPROVED HOMEOPATHIC

Packages

37662-0686-1 — 200 PELLET in 1 VIAL, GLASS (37662-0686-1)

37662-0686-2 — 500 PELLET in 1 VIAL, GLASS (37662-0686-2)

37662-0686-3 — 3000 PELLET in 1 BOTTLE, GLASS (37662-0686-3)

37662-0686-4 — 10000 PELLET in 1 BOTTLE, GLASS (37662-0686-4)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

0220-1937 — EUCALYPTUS GLOBULUS LEAF, 0220-1940 — EUCALYPTUS GLOBULUS LEAF, 37662-0681 — Eucalyptus Globulus, 37662-0682 — Eucalyptus Globulus, 37662-0683 — Eucalyptus Globulus, 37662-0684 — Eucalyptus Globulus, 37662-0685 — Eucalyptus Globulus, 37662-0687 — Eucalyptus Globulus, 50231-221 — MENTHOL, METHYL SALICYLATE, EUCALUPTUS, 55910-192 — Eucalyptus globulus, Natrum muriaticum, 62106-1114 — Allium cepa, Aurum metallicum, Eucalyptus globulus, Inula helenium, Trigonella foenum-graecum, 63083-2170 — Bronchitis Drops, 63083-9201 — Aconitum Combination, 70994-109 — Calendula, Eucalyptus,Peppermint, 72238-004 — Eucalyptus globulus, Natrum muriaticum, 83027-0094 — Eucalyptus Globulus, Lung (Bovine), Sanguinaria Canadensis, Adrenalinum, Belladonna, 83819-030 — Eucalyptus Globulus

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