Youmi Alcohol Prep Pad 70 Isopropyl Alcohol Liquid
NDC Package 87401-000-00

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

Package Information

Youmi Alcohol Prep Pad 70 Isopropyl Alcohol (isopropyl alcohol) liquids is wipe injection site vigorously and discard. This formulation utilizes a liquid delivery system. Marketed by Pt Youmi Medika Industri, this product is identified by NDC 87401-000 and is authorized under FDA application 505G(a)(3).

Identification & Billing

NDC Package Code
87401-000-00
Package Description
.34 mL in 1 POUCH
Product Code
87401-000
11-Digit Billing Format
87401000000
RxNorm Crosswalk

Clinical Specifications

Proprietary Name
Youmi Alcohol Prep Pad 70 Isopropyl Alcohol
Non-Proprietary Name
Isopropyl Alcohol
Substance Name
Isopropyl Alcohol
Dosage Form
Liquid - A dosage form consisting of a pure chemical in its liquid1 state. This dosage form term should not be applied to solutions.
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)
ISOPROPYL ALCOHOL 70 mL/100mL
Usage Information
Wipe injection site vigorously and discard.

Regulatory & Marketing

Labeler Name
Pt Youmi Medika Industri
Product Type
Human Otc Drug
FDA Application #
505G(a)(3)
Marketing Category
OTC MONOGRAPH DRUG -
Start Marketing Date
02-05-2026
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 87401-000-00 identifies a specific commercial package of .34 ml in 1 pouch of Youmi Alcohol Prep Pad 70 Isopropyl Alcohol, a human over the counter drug labeled by Pt Youmi Medika Industri. This liquid is formulated for topical use and contains isopropyl 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 Pt Youmi Medika Industri on February 05, 2026. The current certification is valid through December 31, 2027.

How is this Pt Youmi Medika Industri product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 87401000000. 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)
87401-000-00
11-Digit CMS (5-4-2)
87401-0000-00

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