68647-182 NDC - INFLAMMAGO (ARNICA , DULCAMARA, BRYONIA , BERBERIS , RHUS TOX)

Drug Information

Product NDC: 68647-182

Proprietary Name: Inflammago

Non Proprietary Name: Arnica , Dulcamara, Bryonia , Berberis , Rhus tox

Active Ingredient(s):
  • 6 [hp_C]/40mL ARNICA ANGUSTIFOLIA FLOWER;
  • 6 [hp_C]/40mL BERBERIS VULGARIS FRUIT;
  • 6 [hp_C]/40mL BRYONIA ALBA ROOT;
  • 6 [hp_C]/40mL SOLANUM DULCAMARA FLOWER;
  • 30 [hp_C]/40mL TOXICODENDRON PUBESCENS LEAF


Administration Route(s): ORAL

Dosage Form(s): TINCTURE

Labeler Information

Labeler Name: Feelgood Health
Product Type: HUMAN OTC DRUG
FDA Application Number:
Marketing Category: UNAPPROVED HOMEOPATHIC
Start Marketing Date:1/1/2010

Package Information

No. Package Code Package Description
1 68647-182-10 50000 mL in 1 BOTTLE, GLASS (68647-182-10)

NDC Record

No. Field Name Field Value Field Definition
1 PRODUCT NDC 68647-182 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.
2 PRODUCT TYPE NAME HUMAN OTC DRUG Indicates the type of product, such as Human Prescription Drug or Human OTC Drug. This data element corresponds to the “Document Type” of the SPL submission for the listing.
3 PROPRIETARY NAME Inflammago Also known as the trade name. It is the name of the product chosen by the labeler.
4 NON PROPRIETARY NAME Arnica , Dulcamara, Bryonia , Berberis , Rhus tox Sometimes called the generic name, this is usually the active ingredient(s) of the product.
5 DOSAGE FORM NAME TINCTURE The translation of the DosageForm Code submitted by the firm.
6 ROUTE NAME ORAL The translation of the Route Code submitted by the firm, indicating route of administration.
7 START MARKETING DATE 1/1/2010 This is the date that the labeler indicates was the start of its marketing of the drug product.
8 MARKETING CATEGORY NAME UNAPPROVED HOMEOPATHIC 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.
9 LABELER NAME Feelgood Health Name of Company corresponding to the labeler code segment of the Product NDC.
10 SUBSTANCE NAME ARNICA ANGUSTIFOLIA FLOWER; BERBERIS VULGARIS FRUIT; BRYONIA ALBA ROOT; SOLANUM DULCAMARA FLOWER; TOXICODENDRON PUBESCENS LEAF This is the active ingredient list. Each ingredient name is the preferred term of the UNII code submitted.
11 ACTIVE NUMERATOR STRENGTH 6; 6; 6; 6; 30
12 ACTIVE INGRED UNIT [hp_C]/40mL; [hp_C]/40mL; [hp_C]/40mL; [hp_C]/40mL; [hp_C]/40mL

Download Record

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: 6/12/2015