NDC Package 65753-110-23 Coretex Sun X Spf 30 New

Avobenzone,Homosalate,Octisalate,Octocrylene Lotion Topical - 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:
65753-110-23
Package Description:
50 PACKET in 1 CONTAINER / 7 mL in 1 PACKET
Product Code:
Proprietary Name:
Coretex Sun X Spf 30 New
Non-Proprietary Name:
Avobenzone, Homosalate, Octisalate, Octocrylene
Substance Name:
Avobenzone; Homosalate; Octisalate; Octocrylene
Usage Information:
Put enough product in your palm to cover hands and rub hands together briskly until dry.
11-Digit NDC Billing Format:
65753011023
NDC to RxNorm Crosswalk:
  • RxCUI: 1039474 - ethanol 62.5 % Topical Solution
  • RxCUI: 1039474 - ethanol 0.625 ML/ML Topical Solution
  • RxCUI: 1043353 - benzocaine 6 % Medicated Pad
  • RxCUI: 1043353 - benzocaine 60 MG/ML Medicated Pad
  • RxCUI: 1043353 - benzocaine 6 % Medicated Wipe
  • Product Type:
    Human Otc Drug
    Labeler Name:
    Coretex Products Inc
    Dosage Form:
    Lotion - An emulsion, liquid1 dosage form. This dosage form is generally for external application to the skin.2
    Administration Route(s):
  • Topical - Administration to a particular spot on the outer surface of the body. The E2B term TRANSMAMMARY is a subset of the term TOPICAL.
  • Sample Package:
    No
    FDA Application Number:
    M020
    Marketing Category:
    OTC MONOGRAPH DRUG -
    Start Marketing Date:
    01-07-2021
    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.

    Other Product Packages

    The following packages are also available for this product:

    NDC Package CodePackage Description
    65753-110-0130 mL in 1 BOTTLE, PLASTIC
    65753-110-0259 mL in 1 BOTTLE, PLASTIC
    65753-110-03118 mL in 1 BOTTLE, PLASTIC
    65753-110-04177 mL in 1 BOTTLE, PLASTIC
    65753-110-05236 mL in 1 BOTTLE, PLASTIC
    65753-110-07473 mL in 1 BOTTLE, PLASTIC
    65753-110-081 BAG in 1 BOX / 500 mL in 1 BAG
    65753-110-09946 mL in 1 BOTTLE, PLASTIC
    65753-110-103785 mL in 1 BOTTLE, PLASTIC
    65753-110-181000 PACKET in 1 CARTON / 44 mL in 1 PACKET
    65753-110-2225 PACKET in 1 CONTAINER / 7 mL in 1 PACKET
    65753-110-2450 PACKET in 1 CARTON / 7 mL in 1 PACKET
    65753-110-25100 PACKET in 1 CARTON / 7 mL in 1 PACKET
    65753-110-26300 PACKET in 1 BOX / 7 mL in 1 PACKET
    65753-110-3244 mL in 1 BOTTLE, PLASTIC
    65753-110-3359 mL in 1 BOTTLE, PLASTIC
    65753-110-34118 mL in 1 BOTTLE, PLASTIC
    65753-110-35751 mL in 1 BOTTLE
    65753-110-3744 mL in 1 PACKET

    * Please review the disclaimer below.

    Frequently Asked Questions

    What is NDC 65753-110-23?

    The NDC Packaged Code 65753-110-23 is assigned to a package of 50 packet in 1 container / 7 ml in 1 packet of Coretex Sun X Spf 30 New, a human over the counter drug labeled by Coretex Products Inc. The product's dosage form is lotion and is administered via topical form.

    Is NDC 65753-110 included in the NDC Directory?

    Yes, Coretex Sun X Spf 30 New with product code 65753-110 is active and included in the NDC Directory. The product was first marketed by Coretex Products Inc on January 07, 2021 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 65753-110-23?

    The 11-digit format is 65753011023. 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
    5-3-265753-110-235-4-265753-0110-23