NDC Package 52993-127-06 Zinka Spf 30 Clear Sunscreen

Avobenzone 3%,Homosalate 15%,Octisalate 5%,Octocrylene 8% 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:
52993-127-06
Package Description:
170 g in 1 CAN
Product Code:
Proprietary Name:
Zinka Spf 30 Clear Sunscreen
Non-Proprietary Name:
Avobenzone 3%, Homosalate 15%, Octisalate 5%, Octocrylene 8%
Substance Name:
Avobenzone; Homosalate; Octisalate; Octocrylene
Usage Information:
Apply liberally 15 minutes before sun exposure. Reapply:after 80 minutes of swimming or sweatingimmediately after towel dryingat least every 2 hoursSun protection measures: spending time n the sun increases your risk of skin cancer and early skin aging. To decrease risk, regularly use a sunscreen with broad spectrum SPF of 15 or higher and other sun protection measure including: limit time in the sun, especially from 10 am to 2 pmwear long-sleeved shirts, pants, hats, and sunglasses.Children under 6 months: ask a doctor.Hold container 4 to 6 inches from the skin to apply. Do not spray directly into face. Spray on hands then apply to face. Do no apply in windy conditions. Use in a well-ventilated area.
11-Digit NDC Billing Format:
52993012706
Product Type:
Human Otc Drug
Labeler Name:
Zinka, Inc
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:
    part352
    Marketing Category:
    OTC MONOGRAPH NOT FINAL - A product marketed pursuant to an Over-the-Counter (OTC) Drug Monograph that is not final.
    Start Marketing Date:
    04-19-2021
    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.

    Frequently Asked Questions

    What is NDC 52993-127-06?

    The NDC Packaged Code 52993-127-06 is assigned to a package of 170 g in 1 can of Zinka Spf 30 Clear Sunscreen, a human over the counter drug labeled by Zinka, Inc. The product's dosage form is spray and is administered via topical form.

    Is NDC 52993-127 included in the NDC Directory?

    Yes, Zinka Spf 30 Clear Sunscreen with product code 52993-127 is active and included in the NDC Directory. The product was first marketed by Zinka, Inc on April 19, 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 52993-127-06?

    The 11-digit format is 52993012706. 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
    5-3-252993-127-065-4-252993-0127-06