NDC Package 65753-101-12 Coretex Sun X Spf 30 Thin

Avobenzone,Homosalate,Octinoxate,Octisalate,Oxybenzone Liquid 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:
65753-101-12
Package Description:
118 mL in 1 BOTTLE, SPRAY
Product Code:
Proprietary Name:
Coretex Sun X Spf 30 Thin
Non-Proprietary Name:
Avobenzone, Homosalate, Octinoxate, Octisalate, Oxybenzone
Substance Name:
Avobenzone; Homosalate; Octinoxate; Octisalate; Oxybenzone
Usage Information:
Apply liberally and evenly 15 minutes before sun exposureSun Protection Measures: spending time in the sun increases your risk of skin cancer and early skin aging. To decrease this risk, regularly use a sunscreen with a broad spectrum SPF value of 15 or higher and after sun protection measures including: limit time in the sun, especially from 10:00 a.m. - 2 p.m.wear long-sleeved shirts, pants, hats and sunglasses. reapply:after 80 minutes of swimming or sweatingimmediately after towel dryingat least every 2 hourschildren under 6 months of age: Ask a doctor
11-Digit NDC Billing Format:
65753010112
Product Type:
Human Otc Drug
Labeler Name:
Coretex Products 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):
  • 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:
    11-22-2018
    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
    65753-101-1159 mL in 1 BOTTLE, SPRAY

    * Please review the disclaimer below.

    Frequently Asked Questions

    What is NDC 65753-101-12?

    The NDC Packaged Code 65753-101-12 is assigned to a package of 118 ml in 1 bottle, spray of Coretex Sun X Spf 30 Thin, a human over the counter drug labeled by Coretex Products Inc. The product's dosage form is liquid and is administered via topical form.

    Is NDC 65753-101 included in the NDC Directory?

    Yes, Coretex Sun X Spf 30 Thin with product code 65753-101 is active and included in the NDC Directory. The product was first marketed by Coretex Products Inc on November 22, 2018 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 65753-101-12?

    The 11-digit format is 65753010112. 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
    5-3-265753-101-125-4-265753-0101-12