Label: ARNICA MONTANA tablet
- NDC Code(s): 54973-2904-4
- Packager: Hyland's Inc.
- 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 19, 2022
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- PURPOSE
- ACTIVE INGREDIENT
- INDICATIONS & USAGE
- SPL UNCLASSIFIED SECTION
- Warnings
- Directions
- Inactive ingredients
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- PRINCIPAL DISPLAY PANEL - 250 Tablet Bottle Label
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INGREDIENTS AND APPEARANCE
ARNICA MONTANA
arnica montana tabletProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:54973-2904 Route of Administration ORAL 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 ACACIA (UNII: 5C5403N26O) LACTOSE (UNII: J2B2A4N98G) Product Characteristics Color white (White to Off-White) Score no score Shape ROUND Size 5mm Flavor Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:54973-2904-4 250 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 01/01/1955 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 01/01/1955 Labeler - Hyland's Inc. (008316655) Establishment Name Address ID/FEI Business Operations Hyland's Inc. 008316655 manufacture(54973-2904) , pack(54973-2904)