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  5. NDC Package Code: 82652-021-01 Diphen

NDC Package 82652-021-01 Diphen

Benzocaine,Benzalkonium Chloride,Lidocaine Hydrochloride,Hydrocortisone,Bacitracin - 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:
82652-021-01
Package Description:
1 KIT in 1 CARTON * 1 TABLET, FILM COATED in 1 PACKET (82652-022-01) * 2 TABLET, FILM COATED in 1 PACKET (82652-025-01) * 2 TABLET in 1 PACKET (82652-030-01) * 2 TABLET in 1 PACKET * 1 TABLET, FILM COATED in 1 PACKET (82652-031-01) * 2 TABLET in 1 PACKET (82652-032-01) * 2 TABLET, CHEWABLE in 1 PACKET (82652-026-01) * 2 TABLET, FILM COATED in 1 PACKET (82652-024-01) * 2 TABLET, CHEWABLE in 1 PACKET (82652-023-01) * .5 g in 1 PACKET (82652-028-01) * .9 g in 1 PACKET (82652-027-01) * .9 g in 1 PACKET (82652-029-01) * .75 g in 1 PACKET (82652-033-01)
Product Code:
82652-021
Proprietary Name:
Diphen
Non-Proprietary Name:
Benzocaine, Benzalkonium Chloride, Lidocaine Hydrochloride, Hydrocortisone, Bacitracin Zinc, Neomycin Sulfate, Polymyxin B Sulfate, Calcium Carbonate, Ibuprofen, Loratadine, Acetaminophen, Dextromethorphan Hydrobromide, Guaifenesin, Phenylephrine Hydrochloride, Diphenhydramine Hydrochloride, Potassium Chloride, Magnesium Oxide, Meclizine Hydrochloride, And Bismuth Subsalicylate
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:
82652002101
NDC to RxNorm Crosswalk:
  • RxCUI: 1012100 - benzalkonium chloride 0.13 % / lidocaine HCl 0.5 % Topical Cream
  • RxCUI: 1012100 - benzalkonium chloride 1.3 MG/ML / lidocaine hydrochloride 5 MG/ML Topical Cream
  • RxCUI: 1012100 - benzalkonium chloride 0.13 % / lidocaine hydrochloride 0.5 % Topical Cream
  • RxCUI: 1043690 - hydrocortisone acetate 1 % Topical Cream
  • RxCUI: 1043690 - hydrocortisone acetate 10 MG/ML Topical Cream
    • Product Type:
    Human Otc Drug
    Labeler Name:
    Remedy Pack Llc
    Dosage Form:
    Kit - A packaged collection of related material.
    Sample Package:
    No
    FDA Application Number:
    ANDA076134
    Marketing Category:
    ANDA - A product marketed under an approved Abbreviated New Drug Application.
    Start Marketing Date:
    05-10-2022
    Listing Expiration Date:
    12-31-2024
    Exclude Flag:
    N
    Code Structure:
    • 82652 - Remedy Pack Llc
      • 82652-021 - Diphen
        • 82652-021-01 - 1 KIT in 1 CARTON * 1 TABLET, FILM COATED in 1 PACKET (82652-022-01) * 2 TABLET, FILM COATED in 1 PACKET (82652-025-01) * 2 TABLET in 1 PACKET (82652-030-01) * 2 TABLET in 1 PACKET * 1 TABLET, FILM COATED in 1 PACKET (82652-031-01) * 2 TABLET in 1 PACKET (82652-032-01) * 2 TABLET, CHEWABLE in 1 PACKET (82652-026-01) * 2 TABLET, FILM COATED in 1 PACKET (82652-024-01) * 2 TABLET, CHEWABLE in 1 PACKET (82652-023-01) * .5 g in 1 PACKET (82652-028-01) * .9 g in 1 PACKET (82652-027-01) * .9 g in 1 PACKET (82652-029-01) * .75 g in 1 PACKET (82652-033-01)

    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 82652-021-01?

    The NDC Packaged Code 82652-021-01 is assigned to a package of 1 kit in 1 carton * 1 tablet, film coated in 1 packet (82652-022-01) * 2 tablet, film coated in 1 packet (82652-025-01) * 2 tablet in 1 packet (82652-030-01) * 2 tablet in 1 packet * 1 tablet, film coated in 1 packet (82652-031-01) * 2 tablet in 1 packet (82652-032-01) * 2 tablet, chewable in 1 packet (82652-026-01) * 2 tablet, film coated in 1 packet (82652-024-01) * 2 tablet, chewable in 1 packet (82652-023-01) * .5 g in 1 packet (82652-028-01) * .9 g in 1 packet (82652-027-01) * .9 g in 1 packet (82652-029-01) * .75 g in 1 packet (82652-033-01) of Diphen, a human over the counter drug labeled by Remedy Pack Llc. The product's dosage form is kit and is administered via form.

    Is NDC 82652-021 included in the NDC Directory?

    Yes, Diphen with product code 82652-021 is active and included in the NDC Directory. The product was first marketed by Remedy Pack Llc on May 10, 2022 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 82652-021-01?

    The 11-digit format is 82652002101. 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
    5-3-282652-021-015-4-282652-0021-01