Equate Multi-symptom Relief Eye Drops Solution/ Drops
NDC Package 79903-159-05
Package Information
Equate Multi-symptom Relief Eye Drops (polyethylene glycol 400, tetrahydrozoline hcl, zinc sulfate) solution/ dropses is instill 1 or 2 drops in the affected eye(s) up to 4 times daily children under 6 years of age: ask a doctor. This formulation utilizes a solution/ drops delivery system. Marketed by Walmart, Inc., this product is identified by NDC 79903-159 and is authorized under FDA application M018.
Identification & Billing
- RxCUI: 2360903 - polyethylene glycol 400 1 % / tetrahydrozoline hydrochloride 0.05 % / zinc sulfate 0.25 % Ophthalmic Solution
- RxCUI: 2360903 - polyethylene glycol 400 10 MG/ML / tetrahydrozoline hydrochloride 0.5 MG/ML / zinc sulfate 2.5 MG/ML Ophthalmic Solution
- RxCUI: 2360903 - polyethylene glycol 400 10 MG/ML / tetrahydrozoline hydrochloride 0.5 MG/ML / ZnSO4 2.5 MG/ML Ophthalmic Solution
Clinical Specifications
Regulatory & Marketing
Hierarchy Structure
- 79903 - Walmart, Inc.
- 79903-159 - Equate Multi-symptom Relief Eye Drops
- 79903-159-05 - 1 BOTTLE, DROPPER in 1 BOX / 15 mL in 1 BOTTLE, DROPPER
- 79903-159 - Equate Multi-symptom Relief Eye Drops
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 79903-159-05 identifies a specific commercial package of 1 bottle, dropper in 1 box / 15 ml in 1 bottle, dropper of Equate Multi-symptom Relief Eye Drops, a human over the counter drug labeled by Walmart, Inc.. This solution/ drops is formulated for ophthalmic use and contains polyethylene glycol 400; 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 Walmart, Inc. on February 14, 2023. The current certification is valid through December 31, 2026.
How is this Walmart, Inc. product billed for insurance claims?
For medical billing and reimbursement, this package follows the 11-digit CMS format: 79903015905. 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.