Home NDC 0023-3782 Refresh Relieva PF Xtra
Product NDC 0023-3782
11-digit product format 000233782
Labeler code 0023
Product ID 0023-3782_b6ddb19b-f29a-4a65-ac95-33420c2bd4bf
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 2024-03-01
Substance CARBOXYMETHYLCELLULOSE SODIUM; GLYCERIN
Active strength 5; 9 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 Xtra
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength CARBOXYMETHYLCELLULOSE SODIUM 5 mg/mL GLYCERIN 9 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 RxCUI identifiers# RxCUI identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 1100650 Internal RxNorm 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 0023-3782-10 Refresh Relieva PF Xtra 1 in 1 CARTON SOLUTION/ DROPS 1 5 0023-3782-10 Refresh Relieva PF Xtra 10 mL in 1 BOTTLE, DROPPER SOLUTION/ DROPS 10 5 0023-3782-20 Refresh Relieva PF Xtra 2 in 1 CARTON SOLUTION/ DROPS 2 5 0023-3782-20 Refresh Relieva PF Xtra 10 mL in 1 BOTTLE, DROPPER SOLUTION/ DROPS 10 5 0023-3782-35 Refresh Relieva PF Xtra 1 in 1 CARTON SOLUTION/ DROPS 1 5 0023-3782-35 Refresh Relieva PF Xtra 10 mL in 1 BOTTLE, DROPPER SOLUTION/ DROPS 10 5 0023-3782-50 Refresh Relieva PF Xtra 3.5 mL in 1 BOTTLE, DROPPER SOLUTION/ DROPS 3.5 5 0023-3782-50 Refresh Relieva PF Xtra 1 in 1 CARTON SOLUTION/ DROPS 1 5
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 0023-3782 REFRESH RELIEVA PF XTRA (CARBOXYMETHYLCELLULOSE SODIUM AND GLYCERIN) SOLUTION/ DROPS [ALLERGAN, INC.] 2 Current NDC, 8 package rows 20240608_b51b8a75-8faa-430f-8f7e-ee58d3d13f2e.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 25 of 25 · 486 matching rows.
Brand, Generic, Manufacturer table Brand Generic Manufacturer SPL set ID Effective date Available safety fields Join REFRESH TEARS CARBOXYMETHYLCELLULOSE SODIUM Allergan, Inc. 329d1fe0-4432-4565-b7b1-65666bd86526 2022-06-30 Warnings Exact identifier application number: M018 REFRESH Optive Mega-3 CARBOXYMETHYLCELLULOSE SODIUM, GLYCERIN AND POLYSORBATE 80 Allergan, Inc. c5f2b3f2-2071-45bd-a010-67f848bc0233 2022-06-30 Warnings Exact identifier application number: M018 REFRESH P.M. MINERAL OIL, PETROLATUM Allergan, Inc. 24365d64-cd94-41cc-a7e1-033102d98114 2022-06-30 Warnings Exact identifier application number: M018 REFRESH PLUS CARBOXYMETHYLCELLULOSE SODIUM Allergan, Inc. 0f6a4b4b-cde6-4518-84b5-ce997f1154a7 2022-06-28 Warnings Exact identifier application number: M018 CIRCLE K sterile eye drops TETRAHYDROZOLINE HCL Lil' Drug Store Products, Inc. 2c0e106c-16f6-ff4e-e063-6294a90a7dbb 2018-07-30 Warnings Exact identifier application number: M018 Lil Drug Store Sterile Eye Drops Redness Reliever TETRAHYDROZOLINE HCL Lil' Drug Store Products, Inc. 2c0ea35c-ac52-1043-e063-6394a90a061c 2018-04-30 Warnings Exact identifier application number: M018
DailyMed RxNorm Mappings# Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Marketing start Sample Exclude flag Status 0023-3782-10 00023378210 1 BOTTLE, DROPPER in 1 CARTON (0023-3782-10) / 10 mL in 1 BOTTLE, DROPPER 2024-03-01 No No Current 0023-3782-20 00023378220 2 BOTTLE, DROPPER in 1 CARTON (0023-3782-20) / 10 mL in 1 BOTTLE, DROPPER 2025-10-15 No No Current 0023-3782-35 00023378235 1 BOTTLE, DROPPER in 1 CARTON (0023-3782-35) / 10 mL in 1 BOTTLE, DROPPER 2024-03-01 No No Current 0023-3782-50 00023378250 1 BOTTLE, DROPPER in 1 CARTON (0023-3782-50) / 3.5 mL in 1 BOTTLE, DROPPER 2024-03-01 Yes No Current