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Equisetum Hyemale

NDC 37662-0676 · Hahnemann Laboratories, INC.

Generic nameEquisetum Hyemale
Dosage formPELLET
RouteORAL
Active ingredient(s)EQUISETUM HYEMALE
Strength100 [hp_C]/1
Marketing categoryUNAPPROVED HOMEOPATHIC

Packages

37662-0676-1 — 200 PELLET in 1 VIAL, GLASS (37662-0676-1)

37662-0676-2 — 500 PELLET in 1 VIAL, GLASS (37662-0676-2)

37662-0676-3 — 3000 PELLET in 1 BOTTLE, GLASS (37662-0676-3)

37662-0676-4 — 10000 PELLET in 1 BOTTLE, GLASS (37662-0676-4)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

0220-1885 — EQUISETUM HYEMALE, 0220-1886 — EQUISETUM HYEMALE, 0220-1889 — EQUISETUM HYEMALE, 0220-1890 — EQUISETUM HYEMALE, 0220-1896 — EQUISETUM HYEMALE, 0220-1897 — EQUISETUM HYEMALE, 37662-0673 — Equisetum Hyemale, 37662-0674 — Equisetum Hyemale, 37662-0675 — Equisetum Hyemale, 37662-0677 — Equisetum Hyemale, 37662-0678 — Equisetum Hyemale, 37662-0679 — Equisetum Hyemale, 37662-0680 — Equisetum Hyemale, 58264-0018 — BERBERIS VULGARIS ROOT BARK, LYTTA VESICATORIA, EQUISETUM HYEMALE, EUTROCHIUM PURPUREUM ROOT, and SOLANUM DULCAMARA STEM, 82969-2192 — Berberis vulg, Dulcamara, Equisetum hyemle, Eupatorium purp

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