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  5. NDC Package Code: 66096-115-05 Cough Relief

NDC Package 66096-115-05 Cough Relief

Aconitum Nap,Antimon Crud,Antimon Sulph,Antimon Tart,Aralia Rac,Bryonia,Chelidonium - View Billable Units, 11-Digit Format, RxNorm

Table of Contents

    1. Package Information
    2. Frequently Asked Questions

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:
66096-115-05
Package Description:
59 mL in 1 BOTTLE, SPRAY
Product Code:
66096-115
Proprietary Name:
Cough Relief
Non-Proprietary Name:
Aconitum Nap, Antimon Crud, Antimon Sulph, Antimon Tart, Aralia Rac, Bryonia, Chelidonium Maj, Cuprum Met, Drosera, Hepar Sulph Calc, Kali Carb, Spongia.
Substance Name:
Aconitum Napellus; Antimony Pentasulfide; Antimony Potassium Tartrate; Antimony Trisulfide; Aralia Racemosa Root; Bryonia Alba Root; Calcium Sulfide; Chelidonium Majus; Copper; Drosera Rotundifolia; Potassium Carbonate; Spongia Officinalis Skeleton, Roasted
Usage Information:
This medication is used for temporary relief of coughs without phlegm that are caused by certain infections of the air passages (e.g., sinusitis, common cold). This product should not usually be used for an ongoing cough from smoking or long-term breathing problems (e.g., chronic bronchitis, emphysema) unless directed by your doctor. This product contains dextromethorphan. It is a cough suppressant that works by decreasing the feeling of needing to cough. 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. 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:
66096011505
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.
    • Active Ingredient(s):
  • ACONITUM NAPELLUS 6 [hp_X]/59mL
  • ANTIMONY PENTASULFIDE 8 [hp_X]/59mL
  • ANTIMONY POTASSIUM TARTRATE 8 [hp_X]/59mL
  • ANTIMONY TRISULFIDE 8 [hp_X]/59mL
  • ARALIA RACEMOSA ROOT 4 [hp_X]/59mL
  • BRYONIA ALBA ROOT 6 [hp_X]/59mL
  • CALCIUM SULFIDE 12 [hp_X]/59mL
  • CHELIDONIUM MAJUS 6 [hp_X]/59mL
  • COPPER 12 [hp_X]/59mL
  • DROSERA ROTUNDIFOLIA 6 [hp_X]/59mL
  • POTASSIUM CARBONATE 12 [hp_X]/59mL
  • SPONGIA OFFICINALIS SKELETON, ROASTED 6 [hp_X]/59mL
    • Pharmacologic Class(es):
  • Copper - [CS]
  • Copper-containing Intrauterine Device - [EPC] (Established Pharmacologic Class)
  • Decreased Embryonic Implantation - [PE] (Physiologic Effect)
  • Decreased Sperm Motility - [PE] (Physiologic Effect)
  • Inhibit Ovum Fertilization - [PE] (Physiologic Effect)
    • Sample Package:
    No
    Marketing Category:
    UNAPPROVED HOMEOPATHIC - A category specifying that a product is marketed as unapproved homeopathic product.
    Start Marketing Date:
    05-21-2015
    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 66096-115-05?

    The NDC Packaged Code 66096-115-05 is assigned to a package of 59 ml in 1 bottle, spray of Cough 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 66096-115 included in the NDC Directory?

    Yes, Cough Relief with product code 66096-115 is active and included in the NDC Directory. The product was first marketed by Ohm Pharma Inc. on May 21, 2015 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 66096-115-05?

    The 11-digit format is 66096011505. 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
    5-3-266096-115-055-4-266096-0115-05