68647-182 NDC - INFLAMMAGO (ARNICA , DULCAMARA, BRYONIA , BERBERIS , RHUS TOX)
Product NDC: 68647-182
Proprietary Name: Inflammago
Non Proprietary Name: Arnica , Dulcamara, Bryonia , Berberis , Rhus tox
Administration Route(s): ORAL
Dosage Form(s): TINCTURE
- 6 [hp_C]/40mL ARNICA ANGUSTIFOLIA FLOWER;
- 6 [hp_C]/40mL SOLANUM DULCAMARA FLOWER;
- 6 [hp_C]/40mL BRYONIA ALBA ROOT;
- 6 [hp_C]/40mL BERBERIS VULGARIS FRUIT;
- 30 [hp_C]/40mL TOXICODENDRON PUBESCENS LEAF
||HUMAN OTC DRUG
|FDA Application Number:
|Start Marketing Date:||1/1/2010|
||50000 mL in 1 BOTTLE, GLASS (68647-182-10)
||The labeler code and product code segments of the National Drug Code number, separated by a hyphen. Asterisks are no longer used or included within the product code segment to indicate certain configurations of the NDC.
||PRODUCT TYPE NAME
||HUMAN OTC DRUG
||Indicates the type of product, such as Human Prescription Drug or Human Over the Counter Drug. This data element matches the “Document Type” field of the Structured Product Listing.
||The proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
||NON PROPRIETARY NAME
||Arnica , Dulcamara, Bryonia , Berberis , Rhus tox
||The non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.
||DOSAGE FORM NAME
||The translation of the dosage form Code submitted by the firm.
||The translation of the route code submitted by the firm, indicating route of administration.
||START MARKETING DATE
||This is the date that the labeler indicates was the start of its marketing of the drug product.
||MARKETING CATEGORY NAME
||Product types are broken down into several potential Marketing Categories, such as NDA/ANDA/BLA, OTC Monograph, or Unapproved Drug. One and only one Marketing Category may be chosen for a product, not all marketing categories are available to all product types. Currently, only final marketed product categories are included. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources.
||Name of Company corresponding to the labeler code segment of the Product NDC.
||ARNICA ANGUSTIFOLIA FLOWER; SOLANUM DULCAMARA FLOWER; BRYONIA ALBA ROOT; BERBERIS VULGARIS FRUIT; TOXICODENDRON PUBESCENS LEAF
||This is the active ingredient list. Each ingredient name is the preferred term of the UNII code submitted.
||ACTIVE NUMERATOR STRENGTH
||6; 6; 6; 6; 30
||ACTIVE INGRED UNIT
||[hp_C]/40mL; [hp_C]/40mL; [hp_C]/40mL; [hp_C]/40mL; [hp_C]/40mL
Download this NDC record in Text format: Export
Download this NDC record in Excel (CSV) format: Export
Download this NDC record in XML format: Export
This page was last updated on: 8/2/2017