NDC Package 59088-003-81 Bruselix Bruising

Vitamin C,Zinc,Arnica Montana Extract,Bromelain,Diosmin,Rutin,Citrus - 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:
59088-003-81
Package Description:
14 TABLET in 1 BOTTLE, PLASTIC
Product Code:
Proprietary Name:
Bruselix Bruising
Non-Proprietary Name:
Vitamin C, Zinc, Arnica Montana Extract, Bromelain, Diosmin, Rutin, Citrus Bioflavonoids, Hesperidin Methyl Chalcone
Substance Name:
Arnica Montana Flower; Diosmin; Hesperidin; Hesperidin Methylchalcone; Rutin; Sodium Ascorbate; Stem Bromelain; Zinc Picolinate
Usage Information:
Bruselix™ Bruising Tablets are formulated to provide nutritional support during the body’s natural recovery process. They may be helpful for individuals experiencing bruising due to minor injuries, surgical procedures, or sensitive skin. The formula contains antioxidants, enzymes, and natural extracts that are traditionally used to support overall skin health and recovery.
11-Digit NDC Billing Format:
59088000381
Billing Unit:
EA - Billing unit of "each" is used when the product is dispensed in discreet units.
NDC to RxNorm Crosswalk:
14 EA
Product Type:
Human Prescription Drug
Labeler Name:
Puretek Corporation
Dosage Form:
Tablet - A solid dosage form containing medicinal substances with or without suitable diluents.
Administration Route(s):
Oral - Administration to or by way of the mouth.
Sample Package:
No
Marketing Category:
UNAPPROVED DRUG OTHER - An unapproved drug product in a marketing category that is not reflected on a particular list.
Start Marketing Date:
10-11-2024
Listing Expiration Date:
12-31-2025
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 59088-003-81?

The NDC Packaged Code 59088-003-81 is assigned to a package of 14 tablet in 1 bottle, plastic of Bruselix Bruising, a human prescription drug labeled by Puretek Corporation. The product's dosage form is tablet and is administered via oral form.This product is billed for "EA" each discreet unit and contains an estimated amount of 14 billable units per package.

Is NDC 59088-003 included in the NDC Directory?

Yes, Bruselix Bruising with product code 59088-003 is active and included in the NDC Directory. The product was first marketed by Puretek Corporation on October 11, 2024 and its listing in the NDC Directory is set to expire on December 31, 2025 if the product is not updated or renewed by the manufacturer.

What is the NDC billing unit for package 59088-003-81?

The contents of this package are billed per "each", products billed on a per each basis are usually products dispensed in discreet units. The calculated billable units for this package is 14.

What is the 11-digit format for NDC 59088-003-81?

The 11-digit format is 59088000381. 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
5-3-259088-003-815-4-259088-0003-81