Oxyhives Spray
NDC Package 43695-0010-1

View Billable Units, 11-Digit Conversion Format, and RxNorm mappings
Table of Contents
    1. Package Information
    2. Frequently Asked Questions

Package Information

This product is approaching its end of marketing date. An upcoming end of marketing date means the product has been delisted but will remain in the NDC database until the end of marketing date is reached. In most cases, the FDA advises firms to use the expiration date of the last lot produced as the end marketing date, reflecting the possibility that the product may still be available even after manufacturing has stopped.

Oxyhives (apis mellifica, arnica montana, hepar suis, ichthyolum, lachesis mutus, mercurius solubilis, rhus tox, urtica urens) sprays is relieves symptoms associated with Hives. This formulation utilizes a spray delivery system. Marketed by Global Naturals, Inc., this product is identified by NDC 43695-0010.

Identification & Billing

NDC Package Code
43695-0010-1
Package Description
30 mL in 1 BOTTLE, SPRAY
Product Code
43695-0010
11-Digit Billing Format
43695001001

Clinical Specifications

Proprietary Name
Oxyhives
Non-Proprietary Name
Apis Mellifica, Arnica Montana, Hepar Suis, Ichthyolum, Lachesis Mutus, Mercurius Solubilis, Rhus Tox, Urtica Urens
Substance Name
Apis Mellifera; Arnica Montana; Ichthammol; Lachesis Muta Venom; Mercurius Solubilis; Pork Liver; Toxicodendron Pubescens Leaf; Urtica Urens
Dosage Form
Spray - A liquid minutely divided as by a jet of air or steam.
Administration Route
Oral - Administration to or by way of the mouth.
Active Ingredient(s)
Pharmacologic Class
Usage Information
Relieves symptoms associated with Hives. Relieves symptoms associated with Hives.

Regulatory & Marketing

Labeler Name
Global Naturals, Inc.
Product Type
Human Otc Drug
Marketing Category
UNAPPROVED HOMEOPATHIC - A category specifying that a product is marketed as unapproved homeopathic product.
Start Marketing Date
03-26-2015
End Marketing Date
08-13-2026
Exclude Flag
N
Sample Package
No

Hierarchy Structure

Code Lineage

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 full disclaimer at the bottom of this page.

Frequently Asked Questions

What is the distribution configuration for this product package?

The code 43695-0010-1 identifies a specific commercial package of 30 ml in 1 bottle, spray of Oxyhives, a human over the counter drug labeled by Global Naturals, Inc.. This spray is formulated for oral use and contains apis mellifera; arnica montana; ichthammol; lachesis muta venom; mercurius solubilis; pork liver; toxicodendron pubescens leaf; urtica urens as the active substance.

Is this product currently listed with the FDA?

Yes, this product is active and verified within the NDC Directory. It was introduced to the market by Global Naturals, Inc. on March 26, 2015.

How is this Global Naturals, Inc. product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 43695001001. The table below illustrates the segment conversion from the 10-digit labeler code to the 11-digit provider format.

11-Digit Code Conversion

Billing payers usually require a 5-4-2 segment configuration. Below is the conversion from the 10-digit package format to the 11-digit billing format:

10-Digit Format (5-4-1)
43695-0010-1
11-Digit CMS (5-4-2)
43695-0010-01

Note: The zero is added to the Package segment to maintain the 5-4-2 structure.