Allergy Relief Liquid
NDC Package 66096-710-05

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

Package Information

Allergy Relief (allium cepa, apis mellifica, aralia racemosa, blatta orientalis, bovista, carduus marianus, chelidonium majus, euphrasia officinalas, galphimia glauca, hedera helix, hydrastis canadensis, luffa operculata, nasturtium aquaticum, okoubaka, sabadilla, scrophularia nodosa, solidago virgaurea, taraxacum officinale.) liquids is diphenhydramine is an antihistamine used to relieve symptoms of allergy, hay fever, and the common cold. This formulation utilizes a liquid delivery system. Marketed by Ohm Pharma Inc., this product is identified by NDC 66096-710.

Identification & Billing

NDC Package Code
66096-710-05
Package Description
59 mL in 1 BOTTLE, SPRAY
Product Code
66096-710
11-Digit Billing Format
66096071005

Clinical Specifications

Proprietary Name
Allergy Relief
Non-Proprietary Name
Allium Cepa, Apis Mellifica, Aralia Racemosa, Blatta Orientalis, Bovista, Carduus Marianus, Chelidonium Majus, Euphrasia Officinalas, Galphimia Glauca, Hedera Helix, Hydrastis Canadensis, Luffa Operculata, Nasturtium Aquaticum, Okoubaka, Sabadilla, Scrophularia Nodosa, Solidago Virgaurea, Taraxacum Officinale.
Substance Name
Apis Mellifera; Aralia Racemosa Root; Blatta Orientalis; Chelidonium Majus; Euphrasia Stricta; Galphimia Glauca Flowering Top; Goldenseal; Hedera Helix Flowering Twig; Luffa Operculata Fruit; Lycoperdon Utriforme Fruiting Body; Milk Thistle; Nasturtium Officinale; Okoubaka Aubrevillei Bark; Onion; Schoenocaulon Officinale Seed; Scrophularia Nodosa; Solidago Virgaurea Flowering Top; Taraxacum Officinale
Dosage Form
Liquid - A dosage form consisting of a pure chemical in its liquid1 state. This dosage form term should not be applied to solutions.
Administration Route
Oral - Administration to or by way of the mouth.
Active Ingredient(s)
Pharmacologic Class
Usage Information
Diphenhydramine is an antihistamine used to relieve symptoms of allergy, hay fever, and the common cold. These symptoms include rash, itching, watery eyes, itchy eyes/nose/throat, cough, runny nose, and sneezing. It is also used to prevent and treat nausea, vomiting and dizziness caused by motion sickness. Diphenhydramine can also be used to help you relax and fall asleep. This medication works by blocking a certain natural substance (histamine) that your body makes during an allergic reaction. Its drying effects on such symptoms as watery eyes and runny nose are caused by blocking another natural substance made by your body (acetylcholine). Cough-and-cold products have not been shown to be safe or effective in children younger than 6 years. Therefore, do not use this product to treat cold symptoms in children younger than 6 years unless specifically directed by the doctor. Some products (such as long-acting tablets/capsules) are not recommended for use in children younger than 12 years. Ask your doctor or pharmacist for more details about using your product safely. These products do not cure or shorten the length of the common cold and may cause serious side effects. To decrease the risk for serious side effects, carefully follow all dosage directions. Do not use this product to make a child sleepy. Do not give other cough-and-cold medication that might contain the same or similar ingredients (see also Drug Interactions section). Ask the doctor or pharmacist about other ways to relieve cough and cold symptoms (such as drinking enough fluids, using a humidifier or saline nose drops/spray).

Regulatory & Marketing

Labeler Name
Ohm Pharma 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
06-02-2017
Listing Expiration
12-31-2026
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 66096-710-05 identifies a specific commercial package of 59 ml in 1 bottle, spray of Allergy Relief, a human over the counter drug labeled by Ohm Pharma Inc.. This liquid is formulated for oral use and contains apis mellifera; aralia racemosa root; blatta orientalis; chelidonium majus; euphrasia stricta; galphimia glauca flowering top; goldenseal; hedera helix flowering twig; luffa operculata fruit; lycoperdon utriforme fruiting body; milk thistle; nasturtium officinale; okoubaka aubrevillei bark; onion; schoenocaulon officinale seed; scrophularia nodosa; solidago virgaurea flowering top; taraxacum officinale 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 Ohm Pharma Inc. on June 02, 2017. The current certification is valid through December 31, 2026.

What are the primary indications for this medication?

Diphenhydramine is an antihistamine used to relieve symptoms of allergy, hay fever, and the common cold. These symptoms include rash, itching, watery eyes, itchy eyes/nose/throat, cough, runny nose, and sneezing. It is also used to prevent and treat nausea, vomiting and dizziness caused by motion sickness. Diphenhydramine can also be used to help you relax and fall asleep. This medication works by blocking a certain natural substance (histamine) that your body makes during an allergic reaction. Its drying effects on such symptoms as watery eyes and runny nose are caused by blocking another natural substance made by your body (acetylcholine). Cough-and-cold products have not been shown to be safe or effective in children younger than 6 years. Therefore, do not use this product to treat cold symptoms in children younger than 6 years unless specifically directed by the doctor. Some products (such as long-acting tablets/capsules) are not recommended for use in children younger than 12 years. Ask your doctor or pharmacist for more details about using your product safely. These products do not cure or shorten the length of the common cold and may cause serious side effects. To decrease the risk for serious side effects, carefully follow all dosage directions. Do not use this product to make a child sleepy. Do not give other cough-and-cold medication that might contain the same or similar ingredients (see also Drug Interactions section). Ask the doctor or pharmacist about other ways to relieve cough and cold symptoms (such as drinking enough fluids, using a humidifier or saline nose drops/spray).

How is this Ohm Pharma Inc. product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 66096071005. 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 (5-3-2)
66096-710-05
11-Digit CMS (5-4-2)
66096-0710-05

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