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  5. NDC Package Code: 79265-8065-1 Babo Baby Face Mineral Sunscreen

NDC Package 79265-8065-1 Babo Baby Face Mineral Sunscreen

Mineral Sunscreen Stick 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:
79265-8065-1
Package Description:
1 TUBE in 1 CARTON / 17 g in 1 TUBE
Product Code:
79265-8065
Proprietary Name:
Babo Baby Face Mineral Sunscreen
Non-Proprietary Name:
Mineral Sunscreen
Substance Name:
Zinc Oxide
Usage Information:
This medication is used to treat and prevent diaper rash and other minor skin irritations (e.g., burns, cuts, scrapes). It works by forming a barrier on the skin to protect it from irritants/moisture.
11-Digit NDC Billing Format:
79265806501
Product Type:
Human Otc Drug
Labeler Name:
Babo Botanicals, Inc.
Dosage Form:
Stick - A dosage form prepared in a relatively long and slender often cylindrical form.
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):
  • ZINC OXIDE 20.267 g/100g
    • Sample Package:
    No
    FDA Application Number:
    M020
    Marketing Category:
    OTC MONOGRAPH FINAL - A product marketed pursuant to a final Over-the-Counter (OTC) Drug Monograph.
    Start Marketing Date:
    11-01-2020
    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 79265-8065-1?

    The NDC Packaged Code 79265-8065-1 is assigned to a package of 1 tube in 1 carton / 17 g in 1 tube of Babo Baby Face Mineral Sunscreen, a human over the counter drug labeled by Babo Botanicals, Inc.. The product's dosage form is stick and is administered via topical form.

    Is NDC 79265-8065 included in the NDC Directory?

    Yes, Babo Baby Face Mineral Sunscreen with product code 79265-8065 is active and included in the NDC Directory. The product was first marketed by Babo Botanicals, Inc. on November 01, 2020 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 79265-8065-1?

    The 11-digit format is 79265806501. 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
    5-4-179265-8065-15-4-279265-8065-01