Suntan Cream, Augmented
NDC Package 85421-001-00

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

Package Information

Suntan (suntan lotion) cream is 1.For external use only,Avoid contact with eyes.2.Keep away from babies and children.3.If feel any discomfort after use，please stop using it4.Keep away from fire sources and direct sunlight. This formulation utilizes a cream, augmented delivery system. Marketed by Guangzhou Shangwei Beauty Technologyco.,ltd., this product is identified by NDC 85421-001.

Identification & Billing

NDC Package Code
85421-001-00
Package Description
1 BOTTLE, PLASTIC in 1 BOX, UNIT-DOSE / 1 CREAM, AUGMENTED in 1 BOTTLE, PLASTIC
Product Code
85421-001
11-Digit Billing Format
85421000100

Clinical Specifications

Proprietary Name
Suntan
Non-Proprietary Name
Suntan Lotion
Substance Name
Water
Dosage Form
Cream, Augmented - A cream dosage form that enhances drug delivery. Augmentation does not refer to the strength of the drug in the dosage form. NOTE: CDER has decided to refrain from expanding the use of this dosage form due to difficulties in setting specific criteria that must be met to be considered "augmented”.
Administration Route
Cutaneous - Administration to the skin.
Active Ingredient(s)
WATER 50 g/1001
Usage Information
1.For external use only,Avoid contact with eyes.2.Keep away from babies and children.3.If feel any discomfort after use，please stop using it4.Keep away from fire sources and direct sunlight

Regulatory & Marketing

Labeler Name
Guangzhou Shangwei Beauty Technologyco.,ltd.
Product Type
Human Otc Drug
Marketing Category
UNAPPROVED HOMEOPATHIC - A category specifying that a product is marketed as unapproved homeopathic product.
Start Marketing Date
03-22-2025
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 85421-001-00 identifies a specific commercial package of 1 bottle, plastic in 1 box, unit-dose / 1 cream, augmented in 1 bottle, plastic of Suntan, a human over the counter drug labeled by Guangzhou Shangwei Beauty Technologyco.,ltd.. This cream, augmented is formulated for cutaneous use and contains water 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 Guangzhou Shangwei Beauty Technologyco.,ltd. on March 22, 2025. The current certification is valid through December 31, 2026.

How is this Guangzhou Shangwei Beauty Technologyco.,ltd. product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 85421000100. 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 (5-3-2)
85421-001-00
11-Digit CMS (5-4-2)
85421-0001-00

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