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  5. NDC Package Code: 77039-026-01 Saniiswab

NDC Package 77039-026-01 Saniiswab

Isopropyl Alcohol Liquid Nasal - 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:
77039-026-01
Package Description:
.3 g in 1 POUCH
Product Code:
77039-026
Proprietary Name:
Saniiswab
Non-Proprietary Name:
Isopropyl Alcohol
Substance Name:
Isopropyl Alcohol
Usage Information:
Adults and children over 12 years of age Step 1. Cleaning. Open Step 1 packet and hold handle, inserting one swab tip into each nostril. Swab lower interior lining inside the nose in a circular motion 7 times. Handle guard protects against insertion of swab tip beyond the nostrils. Discard. Step 2. Sanitizing. Repeat Step 1 with Step 2 packet. Discard
11-Digit NDC Billing Format:
77039002601
NDC to RxNorm Crosswalk:
  • RxCUI: 797544 - isopropyl alcohol 70 % Medicated Pad
  • RxCUI: 797544 - isopropyl alcohol 0.7 ML/ML Medicated Pad
  • RxCUI: 797544 - isopropyl alcohol 70 % Topical Cloth
  • RxCUI: 797544 - isopropyl alcohol 70 % Topical Swab
    • Product Type:
    Human Otc Drug
    Labeler Name:
    Ido Pharm
    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):
  • Nasal - Administration to the nose; administered by way of the nose.
    • Active Ingredient(s):
  • ISOPROPYL ALCOHOL 70 mL/100g
    • Sample Package:
    No
    FDA Application Number:
    part333A
    Marketing Category:
    OTC MONOGRAPH NOT FINAL - A product marketed pursuant to an Over-the-Counter (OTC) Drug Monograph that is not final.
    Start Marketing Date:
    09-20-2023
    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 77039-026-01?

    The NDC Packaged Code 77039-026-01 is assigned to a package of .3 g in 1 pouch of Saniiswab, a human over the counter drug labeled by Ido Pharm. The product's dosage form is liquid and is administered via nasal form.

    Is NDC 77039-026 included in the NDC Directory?

    Yes, Saniiswab with product code 77039-026 is active and included in the NDC Directory. The product was first marketed by Ido Pharm on September 20, 2023 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 77039-026-01?

    The 11-digit format is 77039002601. 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
    5-3-277039-026-015-4-277039-0026-01