NDC 53499-3571 – Arnica Montana

Arnica Montana 30 [hp_C]/1 · Tablet · Sublingual

Human Otc Drug

Product NDC53499-3571

Product details

Brand name
Arnica Montana
Generic name
Arnica Montana
Labeler
Schwabe North America, Inc.
Dosage form
Tablet
Route
Sublingual
Marketing category
UNAPPROVED HOMEOPATHIC
Marketed since
January 1, 2006
Marketing end
March 31, 2027

Active ingredients

Uses, dosage, side effects and warnings for Arnica montana →

Package NDC codes (2)

Package NDCDescriptionSince
53499-3571-2100 TABLET in 1 BOTTLE, GLASS (53499-3571-2)Jan 1, 2006
53499-3571-3250 TABLET in 1 BOTTLE, GLASS (53499-3571-3)Jan 1, 2006

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