Medics Choice Eye Drops Seasonal Relief Solution/ Drops
NDC Package 55651-024-01
Package Information
Medics Choice Eye Drops Seasonal Relief (tetrahydrozoline hydrochloride, zinc sulfate) solution/ dropses is instill 1 or 2 drops in the affected eye(s) up to four times daily. This formulation utilizes a solution/ drops delivery system. Marketed by Kc Pharmaceuticals, Inc., this product is identified by NDC 55651-024 and is authorized under FDA application M018.
Identification & Billing
- RxCUI: 1043249 - tetrahydrozoline HCl 0.05 % / zinc sulfate 0.25 % Ophthalmic Solution
- RxCUI: 1043249 - tetrahydrozoline hydrochloride 0.5 MG/ML / zinc sulfate 2.5 MG/ML Ophthalmic Solution
- RxCUI: 1043249 - Tetrahydrozoline hydrochloride 0.5 MG/ML / ZnSO4 2.5 MG/ML Ophthalmic Solution
Clinical Specifications
Regulatory & Marketing
Hierarchy Structure
- 55651 - Kc Pharmaceuticals, Inc.
- 55651-024 - Medics Choice Eye Drops Seasonal Relief
- 55651-024-01 - 1 BOTTLE, DROPPER in 1 CARTON / 15 mL in 1 BOTTLE, DROPPER
- 55651-024 - Medics Choice Eye Drops Seasonal Relief
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 the distribution configuration for this product package?
The code 55651-024-01 identifies a specific commercial package of 1 bottle, dropper in 1 carton / 15 ml in 1 bottle, dropper of Medics Choice Eye Drops Seasonal Relief, a human over the counter drug labeled by Kc Pharmaceuticals, Inc.. This solution/ drops is formulated for ophthalmic use and contains tetrahydrozoline hydrochloride; zinc sulfate 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 Kc Pharmaceuticals, Inc. on October 23, 2003. The current certification is valid through December 31, 2026.
How is this Kc Pharmaceuticals, Inc. product billed for insurance claims?
For medical billing and reimbursement, this package follows the 11-digit CMS format: 55651002401. 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:
Note: The zero is added to the Product segment to maintain the 5-4-2 structure.