NDC 69676-0044 Genexa Arnica Pain

Arnica Montana, Calendula Officinalis, Ledum Palustre, Rhus Toxicodendron, Ruta Graveolens

  1. Labeler Index
  2. Genexa Inc.
  3. NDC: 69676-0044 Genexa Arnica Pain

NDC Product Code 69676-0044

NDC CODE: 69676-0044

Proprietary Name: Genexa Arnica Pain What is the Proprietary Name?
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 Montana, Calendula Officinalis, Ledum Palustre, Rhus Toxicodendron, Ruta Graveolens What is the Non-Proprietary Name?
The non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.

Product Characteristics

Color(s):
WHITE (C48325 - OFF-WHITE)
Shape: ROUND (C48348)
Size(s):
10 MM
Imprint(s):
G
Score: 1
Flavor(s):
GRAPE (C73391)

NDC Code Structure

  • 69676 - Genexa Inc.

NDC 69676-0044-2

Package Description: 1 BOTTLE, PLASTIC in 1 CARTON > 100 TABLET, CHEWABLE in 1 BOTTLE, PLASTIC

NDC Product Information

Genexa Arnica Pain with NDC 69676-0044 is a a human over the counter drug product labeled by Genexa Inc.. The generic name of Genexa Arnica Pain is arnica montana, calendula officinalis, ledum palustre, rhus toxicodendron, ruta graveolens. The product's dosage form is tablet, chewable and is administered via oral form.

Labeler Name: Genexa Inc.

Dosage Form: Tablet, Chewable - A solid dosage form containing medicinal substances with or without suitable diluents that is intended to be chewed, producing a pleasant tasting residue in the oral cavity that is easily swallowed and does not leave a bitter or unpleasant after-taste.

Product Type: Human Otc Drug What kind of product is this?
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.

Genexa Arnica Pain Active Ingredient(s)

What is the Active Ingredient(s) List?
This is the active ingredient list. Each ingredient name is the preferred term of the UNII code submitted.
  • TOXICODENDRON PUBESCENS LEAF 12 [hp_X]/1
  • ARNICA MONTANA 30 [hp_X]/1
  • CALENDULA OFFICINALIS FLOWERING TOP 6 [hp_X]/1
  • LEDUM PALUSTRE TWIG 6 [hp_X]/1
  • RUTA GRAVEOLENS FLOWERING TOP 6 [hp_X]/1

Inactive Ingredient(s)

About the Inactive Ingredient(s)
The inactive ingredients are all the component of a medicinal product OTHER than the active ingredient(s). The acronym "UNII" stands for “Unique Ingredient Identifier” and is used to identify each inactive ingredient present in a product.
  • CARNAUBA WAX (UNII: R12CBM0EIZ)
  • MALTODEXTRIN (UNII: 7CVR7L4A2D)
  • RICE BRAN (UNII: R60QEP13IC)
  • DEXTROSE (UNII: IY9XDZ35W2)

Administration Route(s)

What are the Administration Route(s)?
The translation of the route code submitted by the firm, indicating route of administration.
  • Oral - Administration to or by way of the mouth.

Product Labeler Information

What is the Labeler Name?
Name of Company corresponding to the labeler code segment of the Product NDC.

Labeler Name: Genexa Inc.
Labeler Code: 69676
Marketing Category: UNAPPROVED HOMEOPATHIC - What is the Marketing Category?
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.
Start Marketing Date: 12-20-2020 What is the Start Marketing Date?
This is the date that the labeler indicates was the start of its marketing of the drug product.
Listing Expiration Date: 12-31-2021 What is the Listing Expiration Date?
This is the date when the listing record will expire if not updated or certified by the product labeler.
Exclude Flag: N What is the NDC Exclude Flag?
This field indicates whether the product has been removed/excluded from the NDC Directory for failure to respond to FDA’s requests for correction to deficient or non-compliant submissions. Values = ‘Y’ or ‘N’.

* Please review the disclaimer below.

Genexa Arnica Pain Product Label Images

Genexa Arnica Pain Product Labeling Information

The product labeling information includes all published material associated to a drug. Product labeling documents include information like generic names, active ingredients, ingredient strength dosage, routes of administration, appearance, usage, warnings, inactive ingredients, etc.

Product Labeling Index

Other

Keep outer package for complete product informationDrug Facts

* CLAIMS BASED ON TRADITIONAL HOMEOPATHIC PRACTICE; NOT ACCEPTED MEDICAL EVIDENCE. NOT EVALUATED BY THE FOOD AND DRUG ADMINISTRATION** X is a homeopathic dilution: see genexa.com for more information

Bottle is safety sealed. DO NOT use if bottle seal is disturbed or missing.Patent Pending | Distributed by:Genexa Inc. Atlanta, GA 30318genexa.comCertified Organic by SCS Global Services

Made in the USA with globally sourced ingredientsR-20200828NDC 69676-0044-2

Otc - Active Ingredient

Active ingredients‡**Arnica montana 30X HPUSCalendula officinalis 6X HPUSLedum palustre 6X HPUSRhus toxicodendron 12X HPUSRuta graveolens 6X HPUS‡ Certified Organic"HPUS" indicates that this ingredient is officially included in the Homeopathic Pharmacopoeia of the United States.

Otc - Purpose

Purposetrauma, muscle pain, muscle soreness, stiffness, swelling, bruising, strains and sprainscuts, scrapes and discoloration from bruisingswelling, stiffness and bruisingjoint pain, joint soreness and joint stiffnessmuscle pain and muscle soreness

Indications & Usage

  • Uses*addresses muscle pain and stiffness due to minor injuries, overexertion and falls.addresses pain, swelling and discoloration from bruises.

Warnings

Warnings

Otc - Stop Use

Stop use and ask a doctorif symptoms persist for more than 3 days or worsen.

Otc - Keep Out Of Reach Of Children

Keep out of reach of children.

Otc - Pregnancy Or Breast Feeding

If pregnant or breastfeeding, ask a health professional before use.

Dosage & Administration

  • Directionsadults and children 12 years of ageand olderchew 2 tablets at the onset of symptomsdo not swallow wholerepeat every 4-6 hours as neededchildren 3-11 years of agechew 1 tablet at the onset of symptomsdo not swallow wholerepeat every 4-6 hours as neededchildren under 3 years of ageask a doctor before use

Storage And Handling

Other informationstore between 20-25° C (68-77° F) in a dry place out of direct sunlight

Inactive Ingredient

Inactive ingredientsorganic carnauba wax, organic compliant natural grape flavor, organic maltodextrin, organic rice bran extract, organic tapioca dextrose

Otc - Questions

Questions?1-855-436-3921Mon.-Fri. 7am - 6pm PST

* Please review the disclaimer below.