NDC Package 84010-095-01 Drieyes Lubricant Eye Drops

Carboxymethylcellulose Sodium 0.50% Lubricant Eye Drops Liquid Intraocular - View Billable Units, 11-Digit Format, RxNorm

Package Information

Find all the important details about this NDC Package code, including the 11-Digit NDC Billing number, billing units, wholesale price, RxNorm crosswalk, active ingredients, pharmacologic clasess, etc.

NDC Package Code:
84010-095-01
Package Description:
15 mL in 1 BOTTLE
Product Code:
Proprietary Name:
Drieyes Lubricant Eye Drops
Non-Proprietary Name:
Carboxymethylcellulose Sodium 0.50% Lubricant Eye Drops
Substance Name:
Carboxymethylcellulose Sodium
Usage Information:
This medication is used to relieve dry, irritated eyes. Common causes for dry eyes include wind, sun, heating/air conditioning, computer use/reading, and certain medications. This product may contain 1 or more of the following ingredients: carboxymethylcellulose, dextran, glycerin, hypromellose, polyethylene glycol 400 (PEG 400), polysorbate, polyvinyl alcohol, povidone, or propylene glycol, among others. Eye lubricants keep the eye moist, help to protect the eye from injury and infection, and decrease symptoms of dry eyes such as burning, itching, and feeling as if something is in the eye.
11-Digit NDC Billing Format:
84010009501
NDC to RxNorm Crosswalk:
  • RxCUI: 1188426 - carboxymethylcellulose sodium 0.5 % Ophthalmic Solution
  • RxCUI: 1188426 - carboxymethylcellulose sodium 5 MG/ML Ophthalmic Solution
  • RxCUI: 1188426 - carboxymethylcellulose sodium 0.5 GM per 100 ML Ophthalmic Solution
Product Type:
Human Otc Drug
Labeler Name:
Jiangxi Hemei Pharmaceutical Co., Ltd
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(s):
Intraocular - Administration within the eye.
Sample Package:
No
FDA Application Number:
M018
Marketing Category:
OTC MONOGRAPH DRUG -
Start Marketing Date:
03-28-2025
Listing Expiration Date:
12-31-2026
Exclude Flag:
N

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.

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Frequently Asked Questions

What is NDC 84010-095-01?

The NDC Packaged Code 84010-095-01 is assigned to a package of 15 ml in 1 bottle of Drieyes Lubricant Eye Drops, a human over the counter drug labeled by Jiangxi Hemei Pharmaceutical Co., Ltd. The product's dosage form is liquid and is administered via intraocular form.

Is NDC 84010-095 included in the NDC Directory?

Yes, Drieyes Lubricant Eye Drops with product code 84010-095 is active and included in the NDC Directory. The product was first marketed by Jiangxi Hemei Pharmaceutical Co., Ltd on March 28, 2025 and its listing in the NDC Directory is set to expire on December 31, 2026 if the product is not updated or renewed by the manufacturer.

What is the 11-digit format for NDC 84010-095-01?

The 11-digit format is 84010009501. The 11-digit billing format might be required by the Centers for Medicare & Medicaid Services (CMS) and other payers in billing claim forms.

This package code is originally configured in a 5-3-2 segment 10-digit format and by adding a zero within the original NDC package code we can obtain the converted 11-digit format in a 5-4-2 segment configuration. The table below shows the 11-digit code conversion:

10-Digit Format10-Digit Original Code11-Digit Format11-Digit Code
5-3-284010-095-015-4-284010-0095-01