61096-1039 NDC - BODY BALANCE (ARALIA QUIN, ARNICA, AVENA, CARDUUS MAR, ELAEIS, GLANDULA SUPRARENALIS SUIS, NAT MUR, PHOSPHORICUM AC, THUJA OCC)

Drug Information

Product NDC: 61096-1039

Proprietary Name: Body Balance

Non Proprietary Name: Aralia quin, Arnica, Avena, Carduus mar, Elaeis, Glandula suprarenalis suis, Nat mur, Phosphoricum ac, Thuja occ

Active Ingredient(s):
  • 4 [hp_X]/41mL AMERICAN GINSENG;
  • 4 [hp_X]/41mL ARNICA MONTANA WHOLE;
  • 4 [hp_X]/41mL AVENA SATIVA FLOWERING TOP;
  • 15 [hp_X]/41mL ELAEIS GUINEENSIS FRUIT;
  • 4 [hp_X]/41mL MILK THISTLE;
  • 200 [hp_C]/41mL PHOSPHORIC ACID;
  • 30 [hp_C]/41mL SODIUM CHLORIDE;
  • 12 [hp_X]/41mL SUS SCROFA ADRENAL GLAND;
  • 200 [hp_C]/41mL THUJA OCCIDENTALIS LEAFY TWIG


Administration Route(s): ORAL

Dosage Form(s): LIQUID

Labeler Information

Labeler Name: Eight and Company L.L.C
Product Type: HUMAN OTC DRUG
FDA Application Number:
Marketing Category: UNAPPROVED HOMEOPATHIC
Start Marketing Date:2/28/2019

Package Information

No. Package Code Package Description Billing Unit
161096-1039-11 BOTTLE, SPRAY in 1 CARTON (61096-1039-1) / 41 mL in 1 BOTTLE, SPRAY

NDC Record

Field Name Field Value Definition
PRODUCT NDC61096-1039The 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 NAMEHUMAN OTC DRUGIndicates 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.
PROPRIETARY NAMEBody BalanceThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
NON PROPRIETARY NAMEAralia quin, Arnica, Avena, Carduus mar, Elaeis, Glandula suprarenalis suis, Nat mur, Phosphoricum ac, Thuja occThe non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.
DOSAGE FORM NAMELIQUIDThe translation of the dosage form Code submitted by the firm.
ROUTE NAMEORALThe translation of the route code submitted by the firm, indicating route of administration.
START MARKETING DATE2/28/2019This is the date that the labeler indicates was the start of its marketing of the drug product.
MARKETING CATEGORY NAMEUNAPPROVED HOMEOPATHICProduct 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.
LABELER NAMEEight and Company L.L.CName of Company corresponding to the labeler code segment of the Product NDC.
SUBSTANCE NAMEAMERICAN GINSENG; ARNICA MONTANA WHOLE; AVENA SATIVA FLOWERING TOP; ELAEIS GUINEENSIS FRUIT; MILK THISTLE; PHOSPHORIC ACID; SODIUM CHLORIDE; SUS SCROFA ADRENAL GLAND; THUJA OCCIDENTALIS LEAFY TWIGAn active ingredient is the substance responsible for the medicinal effects of a product specified by the substance's molecular structure or if the molecular structure is not known, defined by an unambiguous definition that identifies the substance. Each active ingredient name is the preferred term of the UNII code submitted.
ACTIVE NUMERATOR STRENGTH4; 4; 4; 15; 4; 200; 30; 12; 200 
ACTIVE INGRED UNIT[hp_X]/41mL; [hp_X]/41mL; [hp_X]/41mL; [hp_X]/41mL; [hp_X]/41mL; [hp_C]/41mL; [hp_C]/41mL; [hp_X]/41mL; [hp_C]/41mL 

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This page was last updated on: 5/3/2024