Home NDC 84938-001 EYE DROPS
Product NDC 84938-001
11-digit product format 849380001
Labeler code 84938
Product ID 84938-001_47373d02-07ae-7104-e063-6294a90a0265
Type HUMAN OTC DRUG
Nonproprietary name Carboxymethylcellulose sodium
Dosage form LIQUID
Route OPHTHALMIC
Labeler Foshan Sugar Max Cosmetics CO.,Ltd
Application M018
Marketing category OTC MONOGRAPH DRUG
Marketing start 2025-12-31
Substance CARBOXYMETHYLCELLULOSE SODIUM, UNSPECIFIED
Active strength .25 g/100mL
NDC exclude flag No
Listing certified through 2026-12-31
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 · 4 matching rows.
View current auxiliary records. · View the auxiliary file history.
Captured / source date, Dataset, Scope table Captured / source date Dataset Scope Package NDC Snapshot Source SHA-256 2025-12-14 17:58 UTC · source 2025-12-05 excluded product product d630ba8d3edf…732f749b63fb…2025-12-14 17:58 UTC · source 2025-12-05 excluded package package 84938-001-01 d630ba8d3edf…732f749b63fb…2025-08-27 00:01 UTC · source 2025-08-26 excluded product product f5e01cc5f278…a2eaf40c39c3…2025-08-27 00:01 UTC · source 2025-08-26 excluded package package 84938-001-01 f5e01cc5f278…a2eaf40c39c3…
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 EYE DROPS
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength CARBOXYMETHYLCELLULOSE SODIUM, UNSPECIFIED .25 g/100mL
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 1547948 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 84938-001-01 EYE DROPS 15 mL in 1 BOTTLE LIQUID 15 3 84938-001-01 EYE DROPS 2 in 1 BOX LIQUID 2 3
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 84938-001 EYE DROPS (CARBOXYMETHYLCELLULOSE SODIUM) LIQUID [FOSHAN SUGAR MAX COSMETICS CO.,LTD] 1 Current NDC, 2 package rows 20241116_26dbf100-593e-3778-e063-6394a90adf26.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 Units Marketing start Sample Exclude flag Status 84938-001-01 84938000101 2 BOTTLE in 1 BOX (84938-001-01) / 15 mL in 1 BOTTLE 2 bottle 2025-12-31 No No Current