Label: ARNICA- arnica montana pellet
- NDC Code(s): 76472-1130-1
- Packager: SEVENE USA
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: unapproved homeopathic
DISCLAIMER: This homeopathic product has not been evaluated by the Food and Drug Administration for safety or efficacy. FDA is not aware of scientific evidence to support homeopathy as effective.
Drug Label Information
Updated September 13, 2023
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- Official Label (Printer Friendly)
- ACTIVE INGREDIENT:
- PURPOSE
- USE:
- DIRECTIONS:
- WARNINGS:
- PREGNANCY OR BREAST FEEDING
- KEEP OUT OF REACH OF CHILDREN
- OTHER INFORMATION:
- DO NOT USE
- INACTIVE INGREDIENTS:
- QUESTIONS?
- PRINCIPAL DISPLAY PANEL
-
INGREDIENTS AND APPEARANCE
ARNICA
arnica montana pelletProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:76472-1130 Route of Administration SUBLINGUAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ARNICA MONTANA (UNII: O80TY208ZW) (ARNICA MONTANA - UNII:O80TY208ZW) ARNICA MONTANA 30 [hp_X] Inactive Ingredients Ingredient Name Strength SUCROSE (UNII: C151H8M554) Product Characteristics Color white Score Shape ROUND Size 4mm Flavor Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:76472-1130-1 80 in 1 CYLINDER; Type 0: Not a Combination Product 11/30/2011 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 11/30/2011 Labeler - SEVENE USA (969332936)