Sunny C Sunscreen Spf 50 Lotion
NDC Package 87611-3245-1

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

Package Information

Sunny C Sunscreen Spf 50 (sunny c sunscreen) lotions is uses- Helps prevent sunburn- if used as directed with other sunprotection measures (see Directions), decreases the risk of skin cancer and early skin aging caused by the sun. This formulation utilizes a lotion delivery system. Marketed by Mixik, Inc., this product is identified by NDC 87611-3245 and is authorized under FDA application M020.

Identification & Billing

NDC Package Code
87611-3245-1
Package Description
1 TUBE in 1 BOX / 50 g in 1 TUBE
Product Code
87611-3245
11-Digit Billing Format
87611324501

Clinical Specifications

Proprietary Name
Sunny C Sunscreen Spf 50
Non-Proprietary Name
Sunny C Sunscreen
Substance Name
Octisalate; Avobenzone; Homosalate; Octinoxate; Octocrylene
Dosage Form
Lotion - An emulsion, liquid1 dosage form. This dosage form is generally for external application to the skin.2
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)
Usage Information
Uses- Helps prevent sunburn- if used as directed with other sunprotection measures (see Directions), decreases the risk of skin cancer and early skin aging caused by the sun.

Regulatory & Marketing

Labeler Name
Mixik, Inc.
Product Type
Human Otc Drug
FDA Application #
M020
Marketing Category
OTC MONOGRAPH DRUG -
Start Marketing Date
03-30-2026
Listing Expiration
12-31-2027
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 87611-3245-1 identifies a specific commercial package of 1 tube in 1 box / 50 g in 1 tube of Sunny C Sunscreen Spf 50, a human over the counter drug labeled by Mixik, Inc.. This lotion is formulated for topical use and contains octisalate; avobenzone; homosalate; octinoxate; octocrylene 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 Mixik, Inc. on March 30, 2026. The current certification is valid through December 31, 2027.

How is this Mixik, Inc. product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 87611324501. 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)
87611-3245-1
11-Digit CMS (5-4-2)
87611-3245-01

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