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  5. NDC Package Code: 61973-112-04 Arizona Sun Spf 45 Surfblok Sunscreen

NDC Package 61973-112-04 Arizona Sun Spf 45 Surfblok Sunscreen

Sunscreen Spray Topical - View Billable Units, 11-Digit Format, RxNorm

Table of Contents

    1. Package Information
    2. Frequently Asked Questions

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:
61973-112-04
Package Description:
120 g in 1 BOTTLE
Product Code:
61973-112
Proprietary Name:
Arizona Sun Spf 45 Surfblok Sunscreen
Non-Proprietary Name:
Sunscreen
Substance Name:
Avobenzone; Homosalate; Octinoxate; Octisalate; Octocrylene; Oxybenzone
Usage Information:
Apply liberally and evenly to the skin 30 minutes before and during sun exposure. Spray into hands and apply to the face. Avoid contact with eyes. Reapply as needed or after towel drying, perspiring, swimming, and vigorous activities. Use on children under six months of age only wih the advise of a physician.
11-Digit NDC Billing Format:
61973011204
Product Type:
Human Otc Drug
Labeler Name:
Arizona Sun Products
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.
    • Active Ingredient(s):
  • AVOBENZONE 30 mg/g
  • HOMOSALATE 100 mg/g
  • OCTINOXATE 75 mg/g
  • OCTISALATE 50 mg/g
  • OCTOCRYLENE 70 mg/g
  • OXYBENZONE 50 mg/g
    • Sample Package:
    No
    FDA Application Number:
    M020
    Marketing Category:
    OTC MONOGRAPH DRUG -
    Start Marketing Date:
    02-21-2024
    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 61973-112-04?

    The NDC Packaged Code 61973-112-04 is assigned to a package of 120 g in 1 bottle of Arizona Sun Spf 45 Surfblok Sunscreen, a human over the counter drug labeled by Arizona Sun Products. The product's dosage form is spray and is administered via topical form.

    Is NDC 61973-112 included in the NDC Directory?

    Yes, Arizona Sun Spf 45 Surfblok Sunscreen with product code 61973-112 is active and included in the NDC Directory. The product was first marketed by Arizona Sun Products on February 21, 2024 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 61973-112-04?

    The 11-digit format is 61973011204. 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
    5-3-261973-112-045-4-261973-0112-04