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  5. NDC Package Code: 84066-101-01 Sunscreen Lip Balm

NDC Package 84066-101-01 Sunscreen Lip Balm

Ethylhexyl Methoxycinnamate,Homosalate,Polysilicone-15,Octocrylene,Butyl - 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:
84066-101-01
Package Description:
3.2 g in 1 TUBE
Product Code:
84066-101
Proprietary Name:
Sunscreen Lip Balm
Non-Proprietary Name:
Ethylhexyl Methoxycinnamate, Homosalate, Polysilicone-15, Octocrylene, Butyl Methoxydibenzoylmethane
Substance Name:
Avobenzone; Homosalate; Octinoxate; Octocrylene; Polysilicone-15
Usage Information:
Helps prevent sumburn if used as directed with other sun protection measures, (see Directions) decreases therisk of skin cancer and early skin aging caused by the sun
11-Digit NDC Billing Format:
84066010101
Product Type:
Human Otc Drug
Labeler Name:
Guangzhou Tata Biotechnology Co., Ltd.
Dosage Form:
Lipstick - A waxy solid, usually colored cosmetic, in stick form for the lips.
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 2 g/100g
  • HOMOSALATE 6 g/100g
  • OCTINOXATE 7 g/100g
  • OCTOCRYLENE 5 g/100g
  • POLYSILICONE-15 5 g/100g
    • Sample Package:
    No
    FDA Application Number:
    M020
    Marketing Category:
    OTC MONOGRAPH DRUG -
    Start Marketing Date:
    01-25-2024
    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 84066-101-01?

    The NDC Packaged Code 84066-101-01 is assigned to a package of 3.2 g in 1 tube of Sunscreen Lip Balm, a human over the counter drug labeled by Guangzhou Tata Biotechnology Co., Ltd.. The product's dosage form is lipstick and is administered via topical form.

    Is NDC 84066-101 included in the NDC Directory?

    Yes, Sunscreen Lip Balm with product code 84066-101 is active and included in the NDC Directory. The product was first marketed by Guangzhou Tata Biotechnology Co., Ltd. on January 25, 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 84066-101-01?

    The 11-digit format is 84066010101. 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
    5-3-284066-101-015-4-284066-0101-01