Sodium Hyaluronate Eye Drops Liquid
NDC Package 87298-037-01

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

Package Information

Sodium Hyaluronate Eye Drops (sodium hyaluronate) liquids is used for dry eye syndrome Relieve dry eye symptoms •The temporary relief of burning and irritation due to dryness of the eye. This formulation utilizes a liquid delivery system. Marketed by Guangzhou Hechuang Commercial Service Co.,ltd., this product is identified by NDC 87298-037 and is authorized under FDA application M018.

Identification & Billing

NDC Package Code
87298-037-01
Package Description
15 g in 1 BOTTLE, PLASTIC
Product Code
87298-037
11-Digit Billing Format
87298003701
RxNorm Crosswalk

Clinical Specifications

Proprietary Name
Sodium Hyaluronate Eye Drops
Non-Proprietary Name
Sodium Hyaluronate
Substance Name
Sodium Hyaluronate
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
Ophthalmic - Administration to the external eye.
Active Ingredient(s)
SODIUM HYALURONATE .1 g/100g
Usage Information
Used for dry eye syndrome Relieve dry eye symptoms •The temporary relief of burning and irritation due to dryness of the eye. •The temporary relief of discomfort due to minor irritations of the eye or exposure to wind or sun. •Use as a protectant against further irritation or to relieve dryness of the eye. •Use as a lubricant to prevent further irritation or to relieve dryness of the eye.

Regulatory & Marketing

Labeler Name
Guangzhou Hechuang Commercial Service Co.,ltd.
Product Type
Human Otc Drug
FDA Application #
M018
Marketing Category
OTC MONOGRAPH DRUG -
Start Marketing Date
05-11-2026
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 87298-037-01 identifies a specific commercial package of 15 g in 1 bottle, plastic of Sodium Hyaluronate Eye Drops, a human over the counter drug labeled by Guangzhou Hechuang Commercial Service Co.,ltd.. This liquid is formulated for ophthalmic use and contains sodium hyaluronate 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 Hechuang Commercial Service Co.,ltd. on May 11, 2026. The current certification is valid through December 31, 2027.

How is this Guangzhou Hechuang Commercial Service Co.,ltd. product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 87298003701. 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)
87298-037-01
11-Digit CMS (5-4-2)
87298-0037-01

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