Los Poblanos Lavender Hand Sanitizer Spray
NDC Package 61577-1110-1

View Billable Units, 11-Digit Conversion Format, and RxNorm mappings

Package Information

Los Poblanos Lavender Hand Sanitizer (alcohol) sprays is helps reduce bacteria on the skin that could cause diseases. This formulation utilizes a spray delivery system. Marketed by Sombra Cosmetics Inc., this product is identified by NDC 61577-1110 and is authorized under FDA application M003.

Identification & Billing

NDC Package Code
61577-1110-1
Package Description
18.2 kg in 1 PAIL
Product Code
11-Digit Billing Format
61577111001

Clinical Specifications

Proprietary Name
Los Poblanos Lavender Hand Sanitizer
Non-Proprietary Name
Alcohol
Substance Name
Alcohol
Dosage Form
Spray - A liquid minutely divided as by a jet of air or steam.
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
Helps reduce bacteria on the skin that could cause diseases.

Regulatory & Marketing

Labeler Name
Sombra Cosmetics Inc.
Product Type
Human Otc Drug
FDA Application #
M003
Marketing Category
OTC MONOGRAPH DRUG -
Start Marketing Date
03-25-2026
Listing Expiration
12-31-2027
Exclude Flag
N
Sample Package
No

Hierarchy 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 full disclaimer at the bottom of this page.

Frequently Asked Questions

What is the distribution configuration for this product package?

The code 61577-1110-1 identifies a specific commercial package of 18.2 kg in 1 pail of Los Poblanos Lavender Hand Sanitizer, a human over the counter drug labeled by Sombra Cosmetics Inc.. This spray is formulated for topical use and contains alcohol 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 Sombra Cosmetics Inc. on March 25, 2026. The current certification is valid through December 31, 2027.

How is this Sombra Cosmetics Inc. product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 61577111001. 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)
61577-1110-1
11-Digit CMS (5-4-2)
61577-1110-01

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