Derma E Sun Drops Spf 30 Lotion
NDC Package 54108-1488-1

11-digit billing NDC: 54108148801
Table of Contents
    1. Package Information
    2. Frequently Asked Questions

Package Information

Derma E Sun Drops Spf 30 (zinc oxide) lotions is shake well before each useApply liberally 15 minutes before sun exposure.Reapply: after 80 minutes of swimming or sweatingimmediately after towel dryingat least every 2 hours when exposed to sunSun Protection Measures. This formulation utilizes a lotion delivery system. Marketed by Derma E, this product is identified by NDC 54108-1488 and is authorized under FDA application M020.

Identification & Billing

NDC Package Code
54108-1488-1
Package Description
1 BOTTLE in 1 BOX / 50 mL in 1 BOTTLE
Product Code
54108-1488
11-Digit Billing Format
54108148801

Clinical Specifications

Proprietary Name
Derma E Sun Drops Spf 30
Non-Proprietary Name
Zinc Oxide
Substance Name
Zinc Oxide
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)
ZINC OXIDE 22 mg/mL
Usage Information
Shake well before each useApply liberally 15 minutes before sun exposure.Reapply: after 80 minutes of swimming or sweatingimmediately after towel dryingat least every 2 hours when exposed to sunSun 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 For children under 6 months: Ask a doctor

Regulatory & Marketing

Labeler Name
Derma E
Product Type
Human Otc Drug
FDA Application #
M020
Marketing Category
OTC MONOGRAPH DRUG -
Start Marketing Date
06-02-2026
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 54108-1488-1 identifies a specific commercial package of 1 bottle in 1 box / 50 ml in 1 bottle of Derma E Sun Drops Spf 30, a human over the counter drug labeled by Derma E. This lotion is formulated for topical use and contains 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 Derma E on June 02, 2026. The current certification is valid through December 31, 2027.

How is this Derma E product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 54108148801. 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)
54108-1488-1
11-Digit CMS (5-4-2)
54108-1488-01

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