Hi-drops
NDC Package 72254-123-01

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

Package Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.

Hi-drops is instill 1 to 2 drops in the affected eye(s) up to four times daily. Marketed by Tiki Talk Llc/hi-drops, this product is identified by NDC 72254-123 and is authorized under FDA application part349.

Identification & Billing

NDC Package Code
72254-123-01
Package Description
1 BOTTLE in 1 BLISTER PACK / 7 mL in 1 BOTTLE
Product Code
72254-123
11-Digit Billing Format
72254012301
RxNorm Crosswalk
  • RxCUI: 1046700 - glycerin 0.25 % / naphazoline HCl 0.012 % Ophthalmic Solution
  • RxCUI: 1046700 - glycerin 2.5 MG/ML / naphazoline hydrochloride 0.12 MG/ML Ophthalmic Solution

Clinical Specifications

Proprietary Name
Hi-drops
Dosage Form
-
Usage Information
Instill 1 to 2 drops in the affected eye(s) up to four times daily.

Regulatory & Marketing

Labeler Name
Tiki Talk Llc/hi-drops
FDA Application #
part349
Marketing Category
OTC MONOGRAPH FINAL - A product marketed pursuant to a final Over-the-Counter (OTC) Drug Monograph.
Start Marketing Date
01-24-2019
Listing Expiration
12-31-2022
Exclude Flag
I
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 72254-123-01 identifies a specific commercial package of 1 bottle in 1 blister pack / 7 ml in 1 bottle of Hi-drops, labeled by Tiki Talk Llc/hi-drops. This is formulated for use and contains as the active substance.

Is this product currently listed with the FDA?

This product code is currently listed as inactive or excluded from the primary directory. It was introduced to the market by Tiki Talk Llc/hi-drops on January 24, 2019. The current certification is valid through December 31, 2022.

How is this Tiki Talk Llc/hi-drops product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 72254012301. 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)
72254-123-01
11-Digit CMS (5-4-2)
72254-0123-01

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