Minidrops Liquid
NDC Package 64108-212-65

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

Package Information

Minidrops (lubricant eye drops) liquids is iNDICATIONS: FOR THE TEMPORARY RELIEF OF BURNING AND IRRITATION DUE TO DRYNESS OF THE EYE.  FOR USE AS A LUBRICANT TO PREVENT FURTHER IRRITATION OR TO RELIEVE DRYNESS OF THE EYE. This formulation utilizes a liquid delivery system. Marketed by Optics Laboratory, Inc, this product is identified by NDC 64108-212 and is authorized under FDA application M018.

Identification & Billing

NDC Package Code
64108-212-65
Package Description
65 VIAL, SINGLE-USE in 1 BOX / .5 mL in 1 VIAL, SINGLE-USE (64108-212-10)
Product Code
64108-212
11-Digit Billing Format
64108021265
RxNorm Crosswalk
  • RxCUI: 1046287 - MiniDrops 1.4 % / 0.6 % Ophthalmic Solution
  • RxCUI: 1046287 - polyvinyl alcohol 0.014 ML/ML / povidone 6 MG/ML Ophthalmic Solution [MiniDrops]
  • RxCUI: 1046287 - MiniDrops (polyvinyl alcohol 1.4 % / povidone 0.6 % ) Ophthalmic Solution
  • RxCUI: 359969 - polyvinyl alcohol 1.4 % / povidone 0.6 % Ophthalmic Solution
  • RxCUI: 359969 - polyvinyl alcohol 0.014 ML/ML / povidone 6 MG/ML Ophthalmic Solution

Clinical Specifications

Proprietary Name
Minidrops
Non-Proprietary Name
Lubricant Eye Drops
Substance Name
Polyvinyl Alcohol; Povidone, Unspecified
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)
Usage Information
INDICATIONS: FOR THE TEMPORARY RELIEF OF BURNING AND IRRITATION DUE TO DRYNESS OF THE EYE.  FOR USE AS A LUBRICANT TO PREVENT FURTHER IRRITATION OR TO RELIEVE DRYNESS OF THE EYE.

Regulatory & Marketing

Labeler Name
Optics Laboratory, Inc
Product Type
Human Otc Drug
FDA Application #
M018
Marketing Category
OTC MONOGRAPH DRUG -
Start Marketing Date
04-01-1991
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.

Other Available Packages

The following commercial packages are registered under the same Product NDC (64108-212). Click a package code to view its specific billing and regulatory data.

64108-212-10
.5 mL in 1 VIAL, SINGLE-USE
64108-212-12
30 VIAL, SINGLE-USE in 1 BOX / .5 mL in 1 VIAL, SINGLE-USE (64108-212-10)
64108-212-13
5 VIAL, SINGLE-USE in 1 BOX / .5 mL in 1 VIAL, SINGLE-USE (64108-212-10)

* 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 64108-212-65 identifies a specific commercial package of 65 vial, single-use in 1 box / .5 ml in 1 vial, single-use (64108-212-10) of Minidrops, a human over the counter drug labeled by Optics Laboratory, Inc. This liquid is formulated for ophthalmic use and contains polyvinyl alcohol; povidone, unspecified 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 Optics Laboratory, Inc on April 01, 1991. The current certification is valid through December 31, 2027.

How is this Optics Laboratory, Inc product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 64108021265. 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)
64108-212-65
11-Digit CMS (5-4-2)
64108-0212-65

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