68703-321 NDC - EYECLEAR PRO ()

Drug Information

Product NDC: 68703-321

Proprietary Name: EyeClear Pro

Non Proprietary Name:

Active Ingredient(s):


Administration Route(s):

Dosage Form(s):

Labeler Information

Labeler Name: Silver Star Brands
Product Type:
FDA Application Number:
Marketing Category:
Start Marketing Date:3/4/2019

Package Information

No. Package Code Package Description Billing Unit
168703-321-0259 mL in 1 BOTTLE, GLASS (68703-321-02)

NDC Record

Field Name Field Value Definition
PRODUCT NDC68703-321The labeler code and product code segments of the National Drug Code number, separated by a hyphen. Asterisks are no longer used or included within the product code segment to indicate certain configurations of the NDC.
PROPRIETARY NAMEEyeClear ProThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE3/4/2019This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAMESilver Star BrandsName of Company corresponding to the labeler code segment of the Product NDC.

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This page was last updated on: 2/19/2021