Mata Hongos Spray
NDC Package 69469-201-01

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

Package Information

Mata Hongos (undecylenic acid) sprays is directionsWash the affected area and dry throughly. This formulation utilizes a spray delivery system. Marketed by Vitamex Usa, Corp, this product is identified by NDC 69469-201 and is authorized under FDA application M005.

Identification & Billing

NDC Package Code
69469-201-01
Package Description
30 mL in 1 BOTTLE, SPRAY
Product Code
11-Digit Billing Format
69469020101

Clinical Specifications

Proprietary Name
Mata Hongos
Non-Proprietary Name
Undecylenic Acid
Substance Name
Undecylenic Acid
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
DirectionsWash the affected area and dry throughly. Apply a thin layer of the product over the affected area twice daily (morning and night) or as directed by a doctor. Pay special attention to spaces between the toes; wear well-fitting ventialted shoes and change shoes and socks at least once daily. This product is not effective on the scalp or nails. Supervise children in the use of this product. DirectionsWash the affected area and dry throughly. Apply a thin layer of the product over the affected area twice daily (morning and night) or as directed by a doctor. Pay special attention to spaces between the toes; wear well-fitting ventialted shoes and change shoes and socks at least once daily. This product is not effective on the scalp or nails. Supervise children in the use of this product.

Regulatory & Marketing

Labeler Name
Vitamex Usa, Corp
Product Type
Human Otc Drug
FDA Application #
M005
Marketing Category
OTC MONOGRAPH DRUG -
Start Marketing Date
09-09-2024
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 69469-201-01 identifies a specific commercial package of 30 ml in 1 bottle, spray of Mata Hongos, a human over the counter drug labeled by Vitamex Usa, Corp. This spray is formulated for topical use and contains undecylenic acid 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 Vitamex Usa, Corp on September 09, 2024. The current certification is valid through December 31, 2026.

How is this Vitamex Usa, Corp product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 69469020101. 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)
69469-201-01
11-Digit CMS (5-4-2)
69469-0201-01

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