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  5. NDC Package Code: 74690-006-01 Dr. C. Tuna Sunscreen 50 Spf Uva Uvb Protection Face And Body Sun

NDC Package 74690-006-01 Dr. C. Tuna Sunscreen 50 Spf Uva Uvb Protection Face And Body Sun

Avobenzone,Octinoxate,Octocrylene,Homosalate Lotion 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:
74690-006-01
Package Description:
75 mL in 1 TUBE
Product Code:
74690-006
Proprietary Name:
Dr. C. Tuna Sunscreen 50 Spf Uva Uvb Protection Face And Body Sun
Non-Proprietary Name:
Avobenzone, Octinoxate, Octocrylene, Homosalate
Substance Name:
Avobenzone; Homosalate; Octinoxate; Octocrylene
Usage Information:
For Sunscreen Use:Apply generously 15 minutes before sun exposure. Reapply at least every 2 hours. Use a water resistant sunscreen if swimming or sweating. Sun Protection Measures: Spending time in the sun increases your risk of skin cancer and early skin aging. To decrease this 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 sunglasses. Children under 6 months: Ask a doctor.
11-Digit NDC Billing Format:
74690000601
Product Type:
Human Otc Drug
Labeler Name:
Farmasi Us Llc
Dosage Form:
Lotion - An emulsion, liquid1 dosage form. This dosage form is generally for external application to the skin.2
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):
Sample Package:
No
FDA Application Number:
M020
Marketing Category:
OTC MONOGRAPH DRUG -
Start Marketing Date:
01-08-2020
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 74690-006-01?

The NDC Packaged Code 74690-006-01 is assigned to a package of 75 ml in 1 tube of Dr. C. Tuna Sunscreen 50 Spf Uva Uvb Protection Face And Body Sun, a human over the counter drug labeled by Farmasi Us Llc. The product's dosage form is lotion and is administered via topical form.

Is NDC 74690-006 included in the NDC Directory?

Yes, Dr. C. Tuna Sunscreen 50 Spf Uva Uvb Protection Face And Body Sun with product code 74690-006 is active and included in the NDC Directory. The product was first marketed by Farmasi Us Llc on January 08, 2020 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 74690-006-01?

The 11-digit format is 74690000601. 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
5-3-274690-006-015-4-274690-0006-01