Private Label Spf 50 80 Min Water Resistant Cream
NDC Package 60232-0035-1

View Billable Units, 11-Digit Conversion Format, and RxNorm mappings
Table of Contents
    1. Package Information
    2. Frequently Asked Questions

Package Information

Private Label Spf 50 80 Min Water Resistant (homosalate, octisalate, zinc oxide sunscreen) cream is apply liberally 15 minutes before sun exposure. This formulation utilizes a cream delivery system. Marketed by Swiss-american Cdmo, Llc, this product is identified by NDC 60232-0035 and is authorized under FDA application M020.

Identification & Billing

NDC Package Code
60232-0035-1
Package Description
1000 g in 1 TUBE
Product Code
60232-0035
11-Digit Billing Format
60232003501

Clinical Specifications

Proprietary Name
Private Label Spf 50 80 Min Water Resistant
Non-Proprietary Name
Homosalate, Octisalate, Zinc Oxide Sunscreen
Substance Name
Homosalate; Octisalate; Zinc Oxide
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
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)
Pharmacologic Class
Usage Information
Apply liberally 15 minutes before sun exposure. Reapply after 80 minutes of swimming or sweating, immediately after towel drying and at least every 2 hours. 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 of 15 or higher and other sun protection measures including: limit time in the sun, especially from 10 am to 2 pm. Wear long-sleeve shirts, pants, hats, and sunglasses. Children under 6 months: ask a physician.

Regulatory & Marketing

Labeler Name
Swiss-american Cdmo, Llc
Product Type
Human Otc Drug
FDA Application #
M020
Marketing Category
OTC MONOGRAPH DRUG -
Start Marketing Date
12-01-2020
Listing Expiration
12-31-2026
Exclude Flag
N
Sample Package
No

Hierarchy Structure

Code Lineage

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 full disclaimer at the bottom of this page.

Frequently Asked Questions

What is the distribution configuration for this product package?

The code 60232-0035-1 identifies a specific commercial package of 1000 g in 1 tube of Private Label Spf 50 80 Min Water Resistant, a human over the counter drug labeled by Swiss-american Cdmo, Llc. This cream is formulated for topical use and contains homosalate; octisalate; zinc oxide as the active substance.

Is this product currently listed with the FDA?

Yes, this product is active and verified within the NDC Directory. It was introduced to the market by Swiss-american Cdmo, Llc on December 01, 2020. The current certification is valid through December 31, 2026.

How is this Swiss-american Cdmo, Llc product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 60232003501. The table below illustrates the segment conversion from the 10-digit labeler code to the 11-digit provider format.

11-Digit Code Conversion

Billing payers usually require a 5-4-2 segment configuration. Below is the conversion from the 10-digit package format to the 11-digit billing format:

10-Digit Format (5-4-1)
60232-0035-1
11-Digit CMS (5-4-2)
60232-0035-01

Note: The zero is added to the Package segment to maintain the 5-4-2 structure.