Symphytum 2004/30/2023 ![]() Each ingredient name is the preferred term of the UNII code submitted. Name of Company corresponding to the labeler code segment of the Product NDC.ĪRNICA MONTANA FLOWER BELLIS PERENNIS COMFREY ROOT DELPHINIUM STAPHISAGRIA SEED ST. The complete list of codes and translations can be found at under Structured Product Labeling Resources. Currently, only final marketed product categories are included. One and only one Marketing Category may be chosen for a product, not all marketing categories are available to all product types. Product types are broken down into several potential Marketing Categories, such as NDA/ANDA/BLA, OTC Monograph, or Unapproved Drug. Ledum 200: when black eyes have a bluish tinged after a few days and Arnica is not helping anymore. This is the date that the labeler indicates was the start of its marketing of the drug product. Boiron Symphytum Officinalis 200ch, 80 pellets, Pure, Green & Safe Pre-Screened Products For All Your Lifestyle Needs + Free shipping on all orders over 25. The translation of the route code submitted by the firm, indicating route of administration. The translation of the dosage form Code submitted by the firm. The generic name usually includes the active ingredient(s) of the product. Symphytum 200c Traditional use by Homeopaths based on Traditional use only Contains approx 50 (7g), 150 (14g) or 250 (25g) Sucrose Pillules Homeopathic medicinal product without approved therapeutic indications Please seek advice from a qualified homeopath for uses and treatments If symptoms worsen or persist, consult a doctor. The non-proprietary name is sometimes called the generic name. It reduces the swelling and pain and promotes union of bones. HYPERICUM,ARNICA,SYMPHYTUM OFFICINALE, BELLIS PERENNIS, STAPHYSAGRIA The proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes. Ingredients: Active Ingredients: Symphytum officinale (HPUS NDC 0220-4857-41) Inactive Ingredients: lactose, sucrose. This product is not intended to diagnose, treat, cure, or prevent any disease. These statements have not been evaluated by the Food and Drug Administration. This data element matches the “Document Type” field of the Structured Product Listing. 5 pellets 3 times a day until symptoms are relieved. Indicates the type of product, such as Human Prescription Drug or Human Over the Counter Drug. Asterisks are no longer used or included within the product code segment to indicate certain configurations of the NDC. The labeler code and product code segments of the National Drug Code number, separated by a hyphen.
0 Comments
Leave a Reply.AuthorWrite something about yourself. No need to be fancy, just an overview. ArchivesCategories |