NDC Package 64760-713-01 Glytone Daily Body

Avobenzone,Octinoxate,Octocrylene,Oxybenzone 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:
64760-713-01
Package Description:
355 mL in 1 BOTTLE, PUMP
Product Code:
Proprietary Name:
Glytone Daily Body
Non-Proprietary Name:
Avobenzone, Octinoxate, Octocrylene, Oxybenzone
Substance Name:
Avobenzone; Octinoxate; Octocrylene; Oxybenzone
Usage Information:
Apply Daily Body Lotion once daily or as directed by a doctor at least 15 minutes before sun exposure.At least every 2 hours apply a sunscreen with broad spectrum SPF 15 or higher for sun protection.Use a water resistant sunscreen if swimming or sweatingSun Protection Measures. Spending time in the sun increases your risk of skin cancer and early skin aging. To decrease the risk, regulatory use a sunscreen with a broad spectrum SPF 15 or higher and other sun protection measures including: limit time in the sun, especially from 10 a.m. - 2 p.m.wear long sleeve shirts, pants, hats, and sunglasses.
11-Digit NDC Billing Format:
64760071301
Product Type:
Human Otc Drug
Labeler Name:
Pierre Fabre Usa 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:
    10-03-2017
    End Marketing Date:
    07-26-2025
    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 64760-713-01?

    The NDC Packaged Code 64760-713-01 is assigned to a package of 355 ml in 1 bottle, pump of Glytone Daily Body, a human over the counter drug labeled by Pierre Fabre Usa Inc.. The product's dosage form is lotion and is administered via topical form.

    Is NDC 64760-713 included in the NDC Directory?

    Yes, Glytone Daily Body with product code 64760-713 is active and included in the NDC Directory. The product was first marketed by Pierre Fabre Usa Inc. on October 03, 2017.

    What is the 11-digit format for NDC 64760-713-01?

    The 11-digit format is 64760071301. 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
    5-3-264760-713-015-4-264760-0713-01