0.9% Benzyl Alcohol Solution (laboratory Use Only) Liquid
NDC Package 87710-002-01

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

Package Information

0.9% Benzyl Alcohol Solution (laboratory Use Only) liquids is for research use only. This formulation utilizes a liquid delivery system. Marketed by Guangzhou Huanmei Cosmetics Co., Ltd, this product is identified by NDC 87710-002.

Identification & Billing

NDC Package Code
87710-002-01
Package Description
1 BOTTLE in 1 BOX / 30 mg in 1 BOTTLE
Product Code
87710-002
11-Digit Billing Format
87710000201

Clinical Specifications

Proprietary Name
0.9% Benzyl Alcohol Solution (laboratory Use Only)
Non-Proprietary Name
0.9% Benzyl Alcohol Solution (laboratory Use Only)
Substance Name
Benzyl 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
Cutaneous - Administration to the skin.
Active Ingredient(s)
BENZYL ALCOHOL .9 mg/100mg
Pharmacologic Class
Pediculicide - [EPC] (Established Pharmacologic Class)
Usage Information
For research use only. Use as required according to the applicable research protocol. The product may be used as a bacteriostatic aqueous solution, solubilizer, penetration aid, or irritation buffer for in vitro research applications. Keep the container sealed after use. Not for injection, skin application, or oral intake.

Regulatory & Marketing

Labeler Name
Guangzhou Huanmei Cosmetics Co., Ltd
Product Type
Human Otc Drug
Marketing Category
UNAPPROVED DRUG OTHER - An unapproved drug product in a marketing category that is not reflected on a particular list.
Start Marketing Date
08-20-2026
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 87710-002-01 identifies a specific commercial package of 1 bottle in 1 box / 30 mg in 1 bottle of 0.9% Benzyl Alcohol Solution (laboratory Use Only), a human over the counter drug labeled by Guangzhou Huanmei Cosmetics Co., Ltd. This liquid is formulated for cutaneous use and contains benzyl 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 Guangzhou Huanmei Cosmetics Co., Ltd on August 20, 2026. The current certification is valid through December 31, 2027.

How is this Guangzhou Huanmei Cosmetics Co., Ltd product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 87710000201. 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)
87710-002-01
11-Digit CMS (5-4-2)
87710-0002-01

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