Label: ACONITE NAPELLIS- aconitum napellus root tablet
- NDC Code(s): 54973-2900-4
- Packager: Hyland's
- 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.
Updated January 13, 2020
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- ACTIVE INGREDIENT
- INDICATIONS & USAGE
- Inactive Ingredients
If you are pregnant or nursing, consult a licensed health care professional before using this product.
- PRINCIPAL DISPLAY PANEL - 250 Tablet Bottle Label
INGREDIENTS AND APPEARANCE
aconitum napellus root tablet
Product Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:54973-2900 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ACONITUM NAPELLUS ROOT (UNII: KPD2N7348X) (ACONITUM NAPELLUS ROOT - UNII:KPD2N7348X) ACONITUM NAPELLUS ROOT 30 [hp_X] Inactive Ingredients Ingredient Name Strength ACACIA (UNII: 5C5403N26O) LACTOSE (UNII: J2B2A4N98G) Product Characteristics Color brown Score no score Shape ROUND Size 9mm Flavor Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:54973-2900-4 250 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 (028570695) Establishment Name Address ID/FEI Business Operations Standard Homeopathic Company 008316655 manufacture(54973-2900) , pack(54973-2900)