carboxymethylcellulose sodium

openFDA label record#

This page contains supplementary openFDA label data. For the canonical label presentation, use the corresponding DailyMed Structured Product Label.

Verified complete openFDA source JSON (canonical bytes are SHA-256 checked before publication)

Brand name: carboxymethylcellulose sodium
Generic name: CARBOXYMETHYLCELLULOSE SODIUM
Manufacturer: AvPAK
Product type: HUMAN OTC DRUG
SPL set ID: b4697319-438e-2ec8-e053-2a95a90abb56
SPL ID: 47e225fb-3d2e-4f80-e063-6394a90aff85
Version: 6
Effective date: 2026-01-08
Source export date: 2026-09-28
Source partition: 6
Source file: https://download.open.fda.gov/drug/label/drug-label-0006-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-09-28/e0861bcde1444ef952820955caafc6f3fd29783e5ade07a13d933aa3336b399f/drug-label-0006-of-0014.json.zip
Source manifest SHA-256: cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run: 20260929T050834Z
Imported at: 2026-09-29 05:35:18

Harmonized routes table
Harmonized routes
OPHTHALMIC

Harmonized identifier links#

Every typed identifier imported from the complete openFDA harmonization object is paginated here; values are not reduced to a first match.

Harmonized identifiers page 1 of 1 · 11 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		M018	openfda.application_number
brand name		carboxymethylcellulose sodium	openfda.brand_name
generic name		CARBOXYMETHYLCELLULOSE SODIUM	openfda.generic_name
manufacturer name		AvPAK	openfda.manufacturer_name
ndc	package	50268-065-30	openfda.package_ndc
ndc	product	50268-065	openfda.product_ndc
ndc11	package	50268006530	derived:openfda.package_ndc
rxcui		579907	openfda.rxcui
spl id		47e225fb-3d2e-4f80-e063-6394a90aff85	id
spl set id		b4697319-438e-2ec8-e053-2a95a90abb56	set_id
unii		K679OBS311	openfda.unii

Warnings cross-check#

openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.

Warnings sections page 1 of 1 · 1 matching rows.

warnings

Warnings For external use only. To avoid contamination, do not touch tip of container to any surface. Do not reuse. Once opened, discard Do not touch unit-dose tip to eye. If solution changes color or becomes cloudy , do not use. Stop use and ask a doctor if you experience eye pain, changes in vision, continued redness or irritation of the eye, or if the condition worsens or persists for more than 72 hours. Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.