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  5. NDC Package Code: 30807-8000-1 Glow Go Lip Oil

NDC Package 30807-8000-1 Glow Go Lip Oil

Avobenzone 30mg/g,Homosalate 100mg/g,Octocrylene 100mg/g,Octisalate 50mg/g,Oil 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:
30807-8000-1
Package Description:
4.5 mL in 1 BOTTLE
Product Code:
30807-8000
Proprietary Name:
Glow Go Lip Oil
Non-Proprietary Name:
Avobenzone 30mg/g, Homosalate 100mg/g, Octocrylene 100mg/g, Octisalate 50mg/g,
Substance Name:
Avobenzone; Homosalate; Octisalate; Octocrylene
Usage Information:
- Apply 20 minutes before sun exposure- Use a water resistant sunscreen if swimming or sweating- Re-apply frequently especially after swimming excercising or towel drying- Re-apply at least every 2 hours- Children under 6 months of age- ask a doctor
11-Digit NDC Billing Format:
30807800001
Product Type:
Human Otc Drug
Labeler Name:
Wild Child Laboratories Pty Ltd
Dosage Form:
Oil - An unctuous, combustible substance which is liquid, or easily liquefiable, on warming, and is soluble in ether but insoluble in water. Such substances, depending on their origin, are classified as animal, mineral, or vegetable oils.
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 3 g/100mL
  • HOMOSALATE 10 g/100mL
  • OCTISALATE 5 g/100mL
  • OCTOCRYLENE 10 g/100mL
    • Sample Package:
    No
    FDA Application Number:
    M020
    Marketing Category:
    OTC MONOGRAPH DRUG -
    Start Marketing Date:
    08-07-2022
    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 30807-8000-1?

    The NDC Packaged Code 30807-8000-1 is assigned to a package of 4.5 ml in 1 bottle of Glow Go Lip Oil, a human over the counter drug labeled by Wild Child Laboratories Pty Ltd. The product's dosage form is oil and is administered via topical form.

    Is NDC 30807-8000 included in the NDC Directory?

    Yes, Glow Go Lip Oil with product code 30807-8000 is active and included in the NDC Directory. The product was first marketed by Wild Child Laboratories Pty Ltd on August 07, 2022 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 30807-8000-1?

    The 11-digit format is 30807800001. 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
    5-4-130807-8000-15-4-230807-8000-01