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  5. NDC Package Code: 53462-110-29 Skin Antisepsis, Oral Cleansing And Nasal Antisepsis System

NDC Package 53462-110-29 Skin Antisepsis, Oral Cleansing And Nasal Antisepsis System

View Billable Units, 11-Digit Format, RxNorm

Table of Contents

    1. Package Information
    2. Frequently Asked Questions

Package Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.

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:
53462-110-29
Package Description:
1 KIT in 1 KIT * 1 PACKET in 1 KIT (53462-375-60) / 7 mL in 1 PACKET * 1 BOTTLE in 1 KIT / 4 mL in 1 BOTTLE (17518-060-04) * 6 PACKAGE in 1 KIT / 6 CLOTH in 1 PACKAGE (53462-705-23)
Product Code:
53462-110
Proprietary Name:
Skin Antisepsis, Oral Cleansing And Nasal Antisepsis System
Usage Information:
Before opening, turn package over, burst solution packet with thumbs. Peel lid to open.Brush teeth and oral cavity for approximately one minute.Instruct to expectorate.Use Applicator Swab for additional cleansing as needed.Discard after use.Use up to 4 times daily or as directed by a dentist or doctor.Children under 12 yeras of age: supervise use.Children under 3 years of age: consult a dentist or doctor.Use a bite block when performing oral care on patients with altered levels of consciousness or those who cannot comprehend commands.Ensure foam is intact after use. If not, remove any particles from oral cavity. use with care in premature infants or infants under 2 months of age. These products may cause irritation or chemical burns.do not microwaveproduct and packaging are not sterile. Follow your hospital policy for skin preparation with non-sterile products.To open packageholding top of package in one hand, lift flap on backside of package with other handgrasp flap at top and pull down to tear flap away and expose foamhold outside of package to present foam and cloths to prep table, avoiding contact between cloths and outside of package to reduce risk of cloth contamination.Orusing sterile scissors, cut off end seal of packagetransfer contents onto prep table, avoiding contact between cloths and outside of package to reduce risk of cloth contaminationuse first cloth to prepare the skin area indicated for a moist or dry site, making certain to keep the second cloth where it will not be contaminated. Use second cloth to prepare larger areas.dry surgical sites (such as abdomen or arm): use one cloth to cleanse each 161 cm² area (approximately 5 x 5 inches) of skin to be prepared. Vigorously scrub skin back and forth for 3 minutes, completely wetting treatment area, then discard. Allow area to air dry for one (1) minute. Do not rinse. moist surgical sites (such as inguinal fold): use one cloth to cleanse each 65 cm² area (approximately 2 x 5 inches) of skin to be prepared. Vigorously scrub skin back and forth for 3 minutes, completely wetting treatment area, then discard. Allow area to air dry for one (1) minute. Do not rinse. discard each cloth after a single useafter package has been opened discard any unused cloths
11-Digit NDC Billing Format:
53462011029
NDC to RxNorm Crosswalk:
  • RxCUI: 1251617 - cetylpyridinium chloride 0.05 % Mouthwash
  • RxCUI: 1251617 - cetylpyridinium chloride 0.5 MG/ML Mouthwash
  • RxCUI: 252965 - povidone-iodine 5 % Topical Solution
  • RxCUI: 252965 - povidone-iodine 50 MG/ML Topical Solution
  • RxCUI: 252965 - povidone-iodine 5 % (titratable iodine 0.5 % ) Topical Solution
    • Labeler Name:
    Sage Products, Llc
    Sample Package:
    No
    Start Marketing Date:
    12-28-2016
    Listing Expiration Date:
    12-31-2018
    Exclude Flag:
    I
    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 53462-110-29?

    The NDC Packaged Code 53462-110-29 is assigned to a package of 1 kit in 1 kit * 1 packet in 1 kit (53462-375-60) / 7 ml in 1 packet * 1 bottle in 1 kit / 4 ml in 1 bottle (17518-060-04) * 6 package in 1 kit / 6 cloth in 1 package (53462-705-23) of Skin Antisepsis, Oral Cleansing And Nasal Antisepsis System, labeled by Sage Products, Llc. The product's dosage form is and is administered via form.

    Is NDC 53462-110 included in the NDC Directory?

    No, Skin Antisepsis, Oral Cleansing And Nasal Antisepsis System with product code 53462-110 is excluded from the NDC Directory because it's listing has been INACTIVATED by FDA. The product was first marketed by Sage Products, Llc on December 28, 2016 and its listing in the NDC Directory is set to expire on December 31, 2018 if the product is not updated or renewed by the manufacturer.

    What is the 11-digit format for NDC 53462-110-29?

    The 11-digit format is 53462011029. 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
    5-3-253462-110-295-4-253462-0110-29