NDC Package 66096-710-05 Allergy Relief

Allium Cepa,Apis Mellifica,Aralia Racemosa,Blatta Orientalis,Bovista,Carduus - 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:
66096-710-05
Package Description:
59 mL in 1 BOTTLE, SPRAY
Product Code:
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
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).
11-Digit NDC Billing Format:
66096071005
Product Type:
Human Otc Drug
Labeler Name:
Ohm Pharma Inc.
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(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:
    06-02-2017
    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 66096-710-05?

    The NDC Packaged Code 66096-710-05 is assigned to a package of 59 ml in 1 bottle, spray of Allergy Relief, a human over the counter drug labeled by Ohm Pharma Inc.. The product's dosage form is liquid and is administered via oral form.

    Is NDC 66096-710 included in the NDC Directory?

    Yes, Allergy Relief with product code 66096-710 is active and included in the NDC Directory. The product was first marketed by Ohm Pharma Inc. on June 02, 2017 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 66096-710-05?

    The 11-digit format is 66096071005. 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
    5-3-266096-710-055-4-266096-0710-05