69842-568 NDC - NIGHTTIME DRY-EYE RELIEF ()

Drug Information

  • Product NDC: 69842-568
  • Proprietary Name: Nighttime Dry-Eye Relief
  • Non Proprietary Name:
  • Active Ingredient(s):
  • Administration Route(s):
  • Dosage Form(s):

Labeler Information

Field Name Field Value
Labeler Name: CVS
Product Type:
FDA Application Number: part349
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date:8/30/2019

Package Information

No. Package Code Package Description Billing Unit
169842-568-131 TUBE in 1 BOX (69842-568-13) / 3.5 g in 1 TUBE

NDC Record

Field Name Field Value Definition
PRODUCT NDC69842-568The 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 NAMENighttime Dry-Eye ReliefThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE8/30/2019This is the date that the labeler indicates was the start of its marketing of the drug product.
MARKETING CATEGORY NAMEOTC MONOGRAPH FINALThe 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.
APPLICATION NUMBERpart349The proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
LABELER NAMECVSThis is the date that the labeler indicates was the start of its marketing of the drug product.

Download Record

Download this NDC record record in Text format: Export

Download this NDC record record in Excel (CSV) format: Export

Download this NDC record record in XML format: Export

This page was last updated on: 11/21/2025

Previous Code
Next Code