NDC Package 14268-025-30 Youth Activating Bb Spf30 Shade 3

Zinc Oxide,Titanium Dioxide Cream 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:
14268-025-30
Package Description:
1 TUBE in 1 CARTON / 30 mL in 1 TUBE
Product Code:
Proprietary Name:
Youth Activating Bb Spf30 Shade 3
Non-Proprietary Name:
Zinc Oxide, Titanium Dioxide
Substance Name:
Titanium Dioxide; Zinc Oxide
Usage Information:
Apply generously 15 minutes before sun exposureChildren under 6 months of age ask a doctorSun Protection Measures. Spending time in the sun increases the risk of skin cancer and early skin aging caused bu the sun. To decrease the risk, regularly use a sunscreen with a Broad Spectrum SPF value of 15 or higher and other sun protection measures including:limit time in the sun, especially from 10 a.m. -2 p.m.wear long-sleeved shirts, pants, hats, and sunglassesReapply at least every 2 hoursUse a water-resistant sunscreen if Simming or sweating
11-Digit NDC Billing Format:
14268002530
Product Type:
Human Otc Drug
Labeler Name:
Englewood Lab, Inc.
Dosage Form:
Cream - An emulsion, semisolid3 dosage form, usually containing > 20% water and volatiles5 and/or < 50% hydrocarbons, waxes, or polyols as the vehicle. This dosage form is generally for external application to the skin or mucous membranes.
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:
M020
Marketing Category:
OTC MONOGRAPH DRUG -
Start Marketing Date:
11-22-2017
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.

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Frequently Asked Questions

What is NDC 14268-025-30?

The NDC Packaged Code 14268-025-30 is assigned to a package of 1 tube in 1 carton / 30 ml in 1 tube of Youth Activating Bb Spf30 Shade 3, a human over the counter drug labeled by Englewood Lab, Inc.. The product's dosage form is cream and is administered via topical form.

Is NDC 14268-025 included in the NDC Directory?

Yes, Youth Activating Bb Spf30 Shade 3 with product code 14268-025 is active and included in the NDC Directory. The product was first marketed by Englewood Lab, Inc. on November 22, 2017 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 14268-025-30?

The 11-digit format is 14268002530. 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
5-3-214268-025-305-4-214268-0025-30