NDC Package 64768-2927-1 Mustela Mineral Sunscreen Broad Spectrum Spf 50

Zinc Oxide,Titanium Dioxide Spray 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:
64768-2927-1
Package Description:
170 g in 1 BOTTLE, SPRAY
Product Code:
Proprietary Name:
Mustela Mineral Sunscreen Broad Spectrum Spf 50
Non-Proprietary Name:
Zinc Oxide, Titanium Dioxide
Substance Name:
Titanium Dioxide; Zinc Oxide
Usage Information:
Shake well before useHold container 4 to 6 inches from the skin to applyApply liberally 15 minutes before sun exposureDo not spray directly into faceDo not spray in windy conditionUse in well-ventilated areaReapply: after 80 minutes of swimming or sweatingimmediately after towel dryingAt least every 2 hours.Sun 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 of 15 or higher and other protection measures including: Limit time in the sun, especially from 10 a.m - 2p.mWear long-sleeved shirt, pants, hat, and sunglassesChildren under 6 months: ask a doctor.
11-Digit NDC Billing Format:
64768292701
Product Type:
Human Otc Drug
Labeler Name:
Expanscience Laboratories D/b/a Mustela
Dosage Form:
Spray - A liquid minutely divided as by a jet of air or steam.
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:
    05-01-2021
    Listing Expiration Date:
    12-31-2024
    Exclude Flag:
    N

    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.

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    Frequently Asked Questions

    What is NDC 64768-2927-1?

    The NDC Packaged Code 64768-2927-1 is assigned to a package of 170 g in 1 bottle, spray of Mustela Mineral Sunscreen Broad Spectrum Spf 50, a human over the counter drug labeled by Expanscience Laboratories D/b/a Mustela. The product's dosage form is spray and is administered via topical form.

    Is NDC 64768-2927 included in the NDC Directory?

    Yes, Mustela Mineral Sunscreen Broad Spectrum Spf 50 with product code 64768-2927 is active and included in the NDC Directory. The product was first marketed by Expanscience Laboratories D/b/a Mustela on May 01, 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 64768-2927-1?

    The 11-digit format is 64768292701. 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 5-4-1 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
    5-4-164768-2927-15-4-264768-2927-01