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  5. NDC Package Code: 85949-113-10 Optiq Balance

NDC Package 85949-113-10 Optiq Balance

Light Mineral Oil,Mineral Oil Emulsion Ophthalmic - View Billable Units, 11-Digit Format, RxNorm

Table of Contents

    1. Package Information
    2. Frequently Asked Questions

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:
85949-113-10
Package Description:
1 VIAL, MULTI-DOSE in 1 CARTON / 10 mL in 1 VIAL, MULTI-DOSE
Product Code:
85949-113
Proprietary Name:
Optiq Balance
Non-Proprietary Name:
Light Mineral Oil, Mineral Oil
Substance Name:
Light Mineral Oil; Mineral Oil
Usage Information:
Shake well before useInstill 1 to 2 drop(s) in the affected eye(s) as needed or as directed by your doctorSee side of carton for directions for use
11-Digit NDC Billing Format:
85949011310
NDC to RxNorm Crosswalk:
  • RxCUI: 2723715 - mineral oil 0.6 % / mineral oil, light 0.6 % Ophthalmic Gel
  • RxCUI: 2723715 - mineral oil 0.006 MG/MG / mineral oil, light 0.006 MG/MG Ophthalmic Gel
  • RxCUI: 2723715 - mineral oil 0.6 % / mineral oil, light 0.6 % Ophthalmic Gel Forming Solution
Product Type:
Human Otc Drug
Labeler Name:
Optiq Eyecare Llc
Dosage Form:
Emulsion - A dosage form consisting of a two-phase system comprised of at least two immiscible liquids1, one of which is dispersed as droplets (internal or dispersed phase) within the other liquid (external or continuous phase), generally stabilized with one or more emulsifying agents. (Note: Emulsion is used as a dosage form term unless a more specific term is applicable, e.g. cream, lotion, ointment.)
Administration Route(s):
Ophthalmic - Administration to the external eye.
Active Ingredient(s):
Sample Package:
No
FDA Application Number:
M018
Marketing Category:
OTC MONOGRAPH DRUG -
Start Marketing Date:
09-20-2025
Listing Expiration Date:
12-31-2026
Exclude Flag:
N
Code Structure:

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 disclaimer below.

Frequently Asked Questions

What is NDC 85949-113-10?

The NDC Packaged Code 85949-113-10 is assigned to a package of 1 vial, multi-dose in 1 carton / 10 ml in 1 vial, multi-dose of Optiq Balance, a human over the counter drug labeled by Optiq Eyecare Llc. The product's dosage form is emulsion and is administered via ophthalmic form.

Is NDC 85949-113 included in the NDC Directory?

Yes, Optiq Balance with product code 85949-113 is active and included in the NDC Directory. The product was first marketed by Optiq Eyecare Llc on September 20, 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 85949-113-10?

The 11-digit format is 85949011310. 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
5-3-285949-113-105-4-285949-0113-10