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Rumex Crispus

NDC 37662-2003 · Hahnemann Laboratories, INC.

Generic nameRumex Crispus
Dosage formPELLET
RouteORAL
Active ingredient(s)RUMEX CRISPUS ROOT
Strength30 [hp_C]/1
Marketing categoryUNAPPROVED HOMEOPATHIC

Packages

37662-2003-1 — 80 PELLET in 1 VIAL, GLASS (37662-2003-1)

37662-2003-2 — 200 PELLET in 1 VIAL, GLASS (37662-2003-2)

37662-2003-3 — 1200 PELLET in 1 BOTTLE, GLASS (37662-2003-3)

37662-2003-4 — 4000 PELLET in 1 BOTTLE, GLASS (37662-2003-4)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

0220-4435 — RUMEX CRISPUS ROOT, 0220-4454 — RUMEX CRISPUS ROOT, 0220-4455 — RUMEX CRISPUS ROOT, 0220-4456 — RUMEX CRISPUS ROOT, 0220-4457 — RUMEX CRISPUS ROOT, 0220-4458 — RUMEX CRISPUS ROOT, 0220-4459 — RUMEX CRISPUS ROOT, 37662-2001 — Rumex Crispus, 37662-2002 — Rumex Crispus, 37662-2004 — Rumex Crispus, 37662-2005 — Rumex Crispus, 37662-2006 — Rumex Crispus, 37662-2007 — Rumex Crispus, 37662-2008 — Rumex Crispus, 37662-2009 — Rumex Crispus

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