Label: ARNICA- arnica montana tablet
- NDC Code(s): 0360-0041-03
- Packager: STANDARD HOMEOPATHIC COMPANY
- 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 December 26, 2018
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- Official Label (Printer Friendly)
- SPL UNCLASSIFIED SECTION
- Warnings
- QUESTIONS
- Directions
- INACTIVE INGREDIENT
- ACTIVE INGREDIENT
- INDICATIONS & USAGE
- Principal Display Panel -- 250 Tablet Bottle Label
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INGREDIENTS AND APPEARANCE
ARNICA
arnica montana tabletProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:0360-0041 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] in 1 g Inactive Ingredients Ingredient Name Strength LACTOSE MONOHYDRATE (UNII: EWQ57Q8I5X) ACACIA (UNII: 5C5403N26O) Product Characteristics Color white Score score with uneven pieces Shape ROUND Size 5mm Flavor Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0360-0041-03 1 g in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 02/17/1997 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 02/17/1997 Labeler - STANDARD HOMEOPATHIC COMPANY (008316655) Establishment Name Address ID/FEI Business Operations STANDARD HOMEOPATHIC COMPANY 008316655 manufacture(0360-0041) , pack(0360-0041) , label(0360-0041)