NDC Package 17089-301-18 Guna-digest

Angelica Archangelica Root - Anisum - Artemisia Abrotanum Flowering Top - Ascorbic Acid - - View Billable Units, 11-Digit Format, RxNorm

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:
17089-301-18
Package Description:
1 BOTTLE, DROPPER in 1 BOX / 30 mL in 1 BOTTLE, DROPPER
Product Code:
Proprietary Name:
Guna-digest
Non-Proprietary Name:
Angelica Archangelica Root - Anisum - Artemisia Abrotanum Flowering Top - Ascorbic Acid - Citrullus Colocynthis Fruit Pulp - Gentiana Lutea Root - Melatonin - Niacin - Pancrelipase Amylase - Pancrelipase Lipase - Pork Liver - Serotonin - Strychnos Nux-vomica Seed - Sus Scrofa Diencephalon - Sus Scrofa Duodenum - Sus Scrofa Gall Bladder - Sus Scrofa Pancreas - Sus Scrofa Pylorus - Thiamine Hydrochloride - Trypsin - Tryptophan -
Substance Name:
Angelica Archangelica Root; Anisum; Artemisia Abrotanum Flowering Top; Ascorbic Acid; Citrullus Colocynthis Fruit Pulp; Gentiana Lutea Root; Melatonin; Niacin; Pancrelipase Amylase; Pancrelipase Lipase; Pork Liver; Serotonin; Strychnos Nux-vomica Seed; Sus Scrofa Diencephalon; Sus Scrofa Duodenum; Sus Scrofa Gallbladder; Sus Scrofa Pancreas; Sus Scrofa Pylorus; Thiamine Hydrochloride; Trypsin; Tryptophan
Usage Information:
Take 15 minutes before mealsAdults and children 12 years and older    20 drops in a little water, 2 times per dayChildren  between 12 years and 6 years of age    10 drops in a little water, 2 times per dayChildren under 6 years     5 drops in a glass of water, 2 times per day
11-Digit NDC Billing Format:
17089030118
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.
Sample Package:
No
Marketing Category:
UNAPPROVED HOMEOPATHIC - A category specifying that a product is marketed as unapproved homeopathic product.
Start Marketing Date:
12-21-2018
Listing Expiration Date:
12-31-2026
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.

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Frequently Asked Questions

What is NDC 17089-301-18?

The NDC Packaged Code 17089-301-18 is assigned to a package of 1 bottle, dropper in 1 box / 30 ml in 1 bottle, dropper of Guna-digest, 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 17089-301 included in the NDC Directory?

Yes, Guna-digest with product code 17089-301 is active and included in the NDC Directory. The product was first marketed by Guna Spa on December 21, 2018 and its listing in the NDC Directory is set to expire on December 31, 2026 if the product is not updated or renewed by the manufacturer.

What is the 11-digit format for NDC 17089-301-18?

The 11-digit format is 17089030118. 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
5-3-217089-301-185-4-217089-0301-18