Home NDC 0023-9537 Refresh RELIEVA PF
Product NDC 0023-9537
11-digit product format 000239537
Labeler code 0023
Product ID 0023-9537_7b606b5f-94b4-49cb-8b26-63c29eafc709
Type HUMAN OTC DRUG
Nonproprietary name Carboxymethylcellulose sodium and Glycerin
Dosage form SOLUTION/ DROPS
Route OPHTHALMIC
Labeler Allergan, Inc.
Application M018
Marketing category OTC MONOGRAPH DRUG
Marketing start 2020-09-25
Substance CARBOXYMETHYLCELLULOSE SODIUM; GLYCERIN
Active strength 5; 10 mg/mL; mg/mL
Pharmacologic classes Allergens [CS], Cell-mediated Immunity [PE], Glycerol [CS], Increased Histamine Release [PE], Increased IgG Production [PE], Non-Standardized Chemical Allergen [EPC]
NDC exclude flag No
Listing certified through 2027-12-31
Current FDA listing Yes Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.
Additional Listing Data#
Finished product Yes
Brand name base Refresh RELIEVA PF
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength CARBOXYMETHYLCELLULOSE SODIUM 5 mg/mL GLYCERIN 10 mg/mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 2 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination K679OBS311 Internal UNII lookup PDC6A3C0OX Internal UNII lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Product Concepts# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 0023-9537-05 Refresh RELIEVA PF 0.4 mL in 1 VIAL, SINGLE-USE SOLUTION/ DROPS 0.4 7 0023-9537-05 Refresh RELIEVA PF 5 in 1 CARTON SOLUTION/ DROPS 5 7
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 0023-9537 REFRESH RELIEVA PF (CARBOXYMETHYLCELLULOSE SODIUM AND GLYCERIN) SOLUTION/ DROPS [ALLERGAN, INC.] 5 Current NDC, Legacy NDC, 2 package rows 20231213_d5d3df4a-a311-4f2d-9a24-edfec1a6c9f9.zip
openFDA label cross-check# OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
Matched openFDA labels page 6 of 25 · 494 matching rows.
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Marketing start Marketing end Sample Exclude flag Status 0023-9537-05 00023953705 5 VIAL, SINGLE-USE in 1 CARTON (0023-9537-05) / .4 mL in 1 VIAL, SINGLE-USE 2020-09-25 0000-00-00 Yes No Current