Home NDC 0023-9205 REFRESH LIQUIGEL
Product NDC 0023-9205
11-digit product format 000239205
Labeler code 0023
Product ID 0023-9205_c0ff3bb9-b271-4607-8623-38e1bc7e3e99
Type HUMAN OTC DRUG
Nonproprietary name Carboxymethylcellulose sodium
Dosage form GEL
Route OPHTHALMIC
Labeler Allergan, Inc.
Application M018
Marketing category OTC MONOGRAPH DRUG
Marketing start 2001-10-04
Substance CARBOXYMETHYLCELLULOSE SODIUM, UNSPECIFIED
Active strength 10 mg/mL
NDC exclude flag No
Listing certified through 2027-12-31
Current FDA listing Yes Observed NDC auxiliary status history# This history shows the information present in each captured FDA auxiliary file. It is not a continuous regulatory timeline, and a missing record does not establish a status.
Historic NDC status page 1 of 1 · 24 matching rows.
View current auxiliary records. · View the auxiliary file history.
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 LIQUIGEL
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength CARBOXYMETHYLCELLULOSE SODIUM, UNSPECIFIED 10 mg/mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination K679OBS311 Internal UNII lookup
Harmonized RxCUI identifiers# RxCUI identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 579907 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 0023-9205-02 REFRESH LIQUIGEL 15 mL in 1 BOTTLE, DROPPER GEL 15 8 0023-9205-02 REFRESH LIQUIGEL 2 in 1 CARTON GEL 2 8 0023-9205-03 REFRESH LIQUIGEL 1 in 1 CARTON GEL 1 8 0023-9205-03 REFRESH LIQUIGEL 3 mL in 1 BOTTLE, DROPPER GEL 3 8 0023-9205-15 REFRESH LIQUIGEL 15 mL in 1 BOTTLE, DROPPER GEL 15 8 0023-9205-15 REFRESH LIQUIGEL 1 in 1 CARTON GEL 1 8
DailyMed Socrata Ingredients# Ingredient, Type, UNII table Ingredient Type UNII DailyMed label SPL version Uploaded Carboxymethylcellulose sodium ACTIVE INGREDIENT K679OBS311 REFRESH LIQUIGEL (CARBOXYMETHYLCELLULOSE SODIUM) GEL [ALLERGAN, INC.] 2 Carboxymethylcellulose ACTIVE MOIETY 05JZI7B19X REFRESH LIQUIGEL (CARBOXYMETHYLCELLULOSE SODIUM) GEL [ALLERGAN, INC.] 2 Boric acid INACTIVE INGREDIENT R57ZHV85D4 REFRESH LIQUIGEL (CARBOXYMETHYLCELLULOSE SODIUM) GEL [ALLERGAN, INC.] 2 calcium chloride INACTIVE INGREDIENT M4I0D6VV5M REFRESH LIQUIGEL (CARBOXYMETHYLCELLULOSE SODIUM) GEL [ALLERGAN, INC.] 2 chlorine dioxide INACTIVE INGREDIENT 8061YMS4RM REFRESH LIQUIGEL (CARBOXYMETHYLCELLULOSE SODIUM) GEL [ALLERGAN, INC.] 2 magnesium chloride INACTIVE INGREDIENT 02F3473H9O REFRESH LIQUIGEL (CARBOXYMETHYLCELLULOSE SODIUM) GEL [ALLERGAN, INC.] 2 potassium chloride INACTIVE INGREDIENT 660YQ98I10 REFRESH LIQUIGEL (CARBOXYMETHYLCELLULOSE SODIUM) GEL [ALLERGAN, INC.] 2 sodium borate INACTIVE INGREDIENT 91MBZ8H3QO REFRESH LIQUIGEL (CARBOXYMETHYLCELLULOSE SODIUM) GEL [ALLERGAN, INC.] 2 sodium chlorate INACTIVE INGREDIENT T95DR77GMR REFRESH LIQUIGEL (CARBOXYMETHYLCELLULOSE SODIUM) GEL [ALLERGAN, INC.] 2 sodium chloride INACTIVE INGREDIENT 451W47IQ8X REFRESH LIQUIGEL (CARBOXYMETHYLCELLULOSE SODIUM) GEL [ALLERGAN, INC.] 2 sodium chlorite INACTIVE INGREDIENT G538EBV4VF REFRESH LIQUIGEL (CARBOXYMETHYLCELLULOSE SODIUM) GEL [ALLERGAN, INC.] 2 water INACTIVE INGREDIENT 059QF0KO0R REFRESH LIQUIGEL (CARBOXYMETHYLCELLULOSE SODIUM) GEL [ALLERGAN, INC.] 2
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 0023-9205 REFRESH LIQUIGEL (CARBOXYMETHYLCELLULOSE SODIUM) GEL [ALLERGAN, INC.] 8 Current NDC, Legacy NDC, 6 package rows 20241113_4b8b2f6a-4b89-446c-9e5b-9b83c453a01d.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.
DailyMed RxNorm Mappings# Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Marketing start Marketing end Sample Exclude flag Status 0023-9205-02 00023920502 2 BOTTLE, DROPPER in 1 CARTON (0023-9205-02) > 15 mL in 1 BOTTLE, DROPPER 2001-10-04 0000-00-00 No No Current 0023-9205-03 00023920503 1 BOTTLE, DROPPER in 1 CARTON (0023-9205-03) > 3 mL in 1 BOTTLE, DROPPER 2001-10-04 0000-00-00 No No Current 0023-9205-15 00023920515 1 BOTTLE, DROPPER in 1 CARTON (0023-9205-15) / 15 mL in 1 BOTTLE, DROPPER 2001-10-04 0000-00-00 No No Current