NDC Package 10967-663-01 Revlon Colorstay Light Cover Foundation

Homosalate,Octisalate,Octocrylene,Titanium Dioxide, Zinc Oxide Emulsion 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:
10967-663-01
Package Description:
1 mL in 1 TUBE
Product Code:
Proprietary Name:
Revlon Colorstay Light Cover Foundation
Non-Proprietary Name:
Homosalate, Octisalate, Octocrylene, Titanium Dioxide, Zinc Oxide
Substance Name:
Homosalate; Octisalate; Octocrylene; Titanium Dioxide; Zinc Oxide
Usage Information:
Apply liberally 15 minutes before sun exposureUse water resistant sunscreen if swimming or sweatingRepply at least every 2 hoursChildren under 6 months: Ask a doctor
11-Digit NDC Billing Format:
10967066301
Product Type:
Human Otc Drug
Labeler Name:
Revlon
Dosage Form:
Emulsion - A dosage form consisting of a two-phase system comprised of at least two immiscible liquids1, one of which is dispersed as droplets (internal or dispersed phase) within the other liquid (external or continuous phase), generally stabilized with one or more emulsifying agents. (Note: Emulsion is used as a dosage form term unless a more specific term is applicable, e.g. cream, lotion, ointment.)
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:
    10-01-2020
    Listing Expiration Date:
    12-31-2025
    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 10967-663-01?

    The NDC Packaged Code 10967-663-01 is assigned to a package of 1 ml in 1 tube of Revlon Colorstay Light Cover Foundation, a human over the counter drug labeled by Revlon. The product's dosage form is emulsion and is administered via topical form.

    Is NDC 10967-663 included in the NDC Directory?

    Yes, Revlon Colorstay Light Cover Foundation with product code 10967-663 is active and included in the NDC Directory. The product was first marketed by Revlon on October 01, 2020 and its listing in the NDC Directory is set to expire on December 31, 2025 if the product is not updated or renewed by the manufacturer.

    What is the 11-digit format for NDC 10967-663-01?

    The 11-digit format is 10967066301. 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
    5-3-210967-663-015-4-210967-0663-01