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  5. NDC Package Code: 17089-463-18 Guna Arthro Relief

NDC Package 17089-463-18 Guna Arthro Relief

Arteria Suis - Alpha Ketoglutaricum Acidum - Alpha Lipoicum Acidum - Ascorbicum Acidum - - View Billable Units, 11-Digit Format, RxNorm

Table of Contents

    1. Package Information
    2. Frequently Asked Questions

Package Information

Find all the important details about this NDC Package code, including the 11-Digit NDC Billing number, billing units, wholesale price, RxNorm crosswalk, active ingredients, pharmacologic clasess, etc.

NDC Package Code:
17089-463-18
Package Description:
1 BOTTLE, DROPPER in 1 BOX / 30 mL in 1 BOTTLE, DROPPER
Product Code:
17089-463
Proprietary Name:
Guna Arthro Relief
Non-Proprietary Name:
Arteria Suis - Alpha Ketoglutaricum Acidum - Alpha Lipoicum Acidum - Ascorbicum Acidum - Barium Oxalsuccinicum - Bryonia Alba - Calcarea Carbonica - Cartilago Suis - Chlorinum - Cimicifuga Racemosa - Colchicum Autumnale - Dulcamara - Embryo Suis - Funiculus Umbilicalis Suis - Glandula Suprarenalis Suis - Nadidum - Natrum Oxalaceticum - Natrum Sulphuricum - Placenta Totalis Suis - Rhus Toxicodendron - Sulphur- Vena Suis -
Substance Name:
.alpha.-ketoglutaric Acid; .alpha.-lipoic Acid; Ascorbic Acid; Barium Oxalosuccinate; Black Cohosh; Bryonia Alba Root; Chlorine; Colchicum Autumnale Bulb; Nadide; Oyster Shell Calcium Carbonate, Crude; Sodium Diethyl Oxalacetate; Sodium Sulfate; Solanum Dulcamara Flower; Sulfur; Sus Scrofa Adrenal Gland; Sus Scrofa Artery; Sus Scrofa Cartilage; Sus Scrofa Embryo; Sus Scrofa Placenta; Sus Scrofa Umbilical Cord; Sus Scrofa Vein; Toxicodendron Pubescens Leaf
Usage Information:
Take 15 minutes before meals
11-Digit NDC Billing Format:
17089046318
Product Type:
Human Otc Drug
Labeler Name:
Guna Spa
Dosage Form:
Solution/ Drops - A solution which is usually administered in a drop-wise fashion.
Administration Route(s):
  • Oral - Administration to or by way of the mouth.
    • Active Ingredient(s):
  • .ALPHA.-KETOGLUTARIC ACID 3 [hp_X]/30mL
  • .ALPHA.-LIPOIC ACID 8 [hp_X]/30mL
  • ASCORBIC ACID 3 [hp_X]/30mL
  • BARIUM OXALOSUCCINATE 6 [hp_X]/30mL
  • BLACK COHOSH 6 [hp_X]/30mL
  • BRYONIA ALBA ROOT 6 [hp_X]/30mL
  • CHLORINE 6 [hp_X]/30mL
  • COLCHICUM AUTUMNALE BULB 6 [hp_X]/30mL
  • NADIDE 3 [hp_X]/30mL
  • OYSTER SHELL CALCIUM CARBONATE, CRUDE 4 [hp_X]/30mL
  • SODIUM DIETHYL OXALACETATE 3 [hp_X]/30mL
  • SODIUM SULFATE 8 [hp_X]/30mL
  • SOLANUM DULCAMARA FLOWER 6 [hp_X]/30mL
  • SULFUR 4 [hp_X]/30mL
  • SUS SCROFA ADRENAL GLAND 6 [hp_X]/30mL
  • SUS SCROFA ARTERY 6 [hp_X]/30mL
  • SUS SCROFA CARTILAGE 6 [hp_X]/30mL
  • SUS SCROFA EMBRYO 6 [hp_X]/30mL
  • SUS SCROFA PLACENTA 6 [hp_X]/30mL
  • SUS SCROFA UMBILICAL CORD 6 [hp_X]/30mL
  • SUS SCROFA VEIN 6 [hp_X]/30mL
  • TOXICODENDRON PUBESCENS LEAF 6 [hp_X]/30mL
    • Pharmacologic Class(es):
  • Ascorbic Acid - [CS]
  • Increased Large Intestinal Motility - [PE] (Physiologic Effect)
  • Inhibition Large Intestine Fluid/Electrolyte Absorption - [PE] (Physiologic Effect)
  • Osmotic Activity - [MoA] (Mechanism of Action)
  • Osmotic Laxative - [EPC] (Established Pharmacologic Class)
  • Vitamin C - [EPC] (Established Pharmacologic Class)
    • Sample Package:
    No
    Marketing Category:
    UNAPPROVED HOMEOPATHIC - A category specifying that a product is marketed as unapproved homeopathic product.
    Start Marketing Date:
    09-24-2020
    Listing Expiration Date:
    12-31-2024
    Exclude Flag:
    N
    Code Structure:

    The NDC Directory contains ONLY information on final marketed drugs submitted to FDA electronically by labelers. A labeler might be a manufacturer, re-packager or re-labeler. The product information included in the NDC directory does not indicate that FDA has verified the information provided by the product labeler. Assigned NDC numbers are not in any way an indication of FDA approval of the product.

    * Please review the disclaimer below.

    Frequently Asked Questions

    What is NDC 17089-463-18?

    The NDC Packaged Code 17089-463-18 is assigned to a package of 1 bottle, dropper in 1 box / 30 ml in 1 bottle, dropper of Guna Arthro Relief, a human over the counter drug labeled by Guna Spa. The product's dosage form is solution/ drops and is administered via oral form.

    Is NDC 17089-463 included in the NDC Directory?

    Yes, Guna Arthro Relief with product code 17089-463 is active and included in the NDC Directory. The product was first marketed by Guna Spa on September 24, 2020 and its listing in the NDC Directory is set to expire on December 31, 2024 if the product is not updated or renewed by the manufacturer.

    What is the 11-digit format for NDC 17089-463-18?

    The 11-digit format is 17089046318. The 11-digit billing format might be required by the Centers for Medicare & Medicaid Services (CMS) and other payers in billing claim forms.

    This package code is originally configured in a 5-3-2 segment 10-digit format and by adding a zero within the original NDC package code we can obtain the converted 11-digit format in a 5-4-2 segment configuration. The table below shows the 11-digit code conversion:

    10-Digit Format10-Digit Original Code11-Digit Format11-Digit Code
    5-3-217089-463-185-4-217089-0463-18