Eyes Alive Lubricating

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: Eyes Alive Lubricating
Generic name: CARBOXYMETHYLCELLULOSE SODIUM, UNSPECIFIED
Manufacturer: RIVIERA PHARMA INC
Product type: HUMAN OTC DRUG
SPL set ID: b6966691-6884-438c-9f89-5924089226e1
SPL ID: 7b0dddfc-9933-4f2f-840f-7a7b28cbf1fa
Version: 3
Effective date: 2024-05-31
Source export date: 2026-09-28
Source partition: 9
Source file: https://download.open.fda.gov/drug/label/drug-label-0009-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-09-28/6784607726c827491ceaeab30d843632e0660ee8008c535197be5ed9e1e52201/drug-label-0009-of-0014.json.zip
Source manifest SHA-256: cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run: 20260929T050834Z
Imported at: 2026-09-29 06:03:18

Harmonized routes table
Harmonized routes
INTRAOCULAR

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 · 24 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		M018	openfda.application_number
brand name		Eyes Alive Lubricating	openfda.brand_name
generic name		CARBOXYMETHYLCELLULOSE SODIUM, UNSPECIFIED	openfda.generic_name
manufacturer name		RIVIERA PHARMA INC	openfda.manufacturer_name
ndc	package	83291-200-02	openfda.package_ndc
ndc	package	83291-200-52	openfda.package_ndc
ndc	package	83291-200-00	openfda.package_ndc
ndc	package	83291-200-08	openfda.package_ndc
ndc	package	83291-200-32	openfda.package_ndc
ndc	package	83291-200-72	openfda.package_ndc
ndc	package	83291-200-04	openfda.package_ndc
ndc	product	83291-200	openfda.product_ndc
ndc11	package	83291020032	derived:openfda.package_ndc
ndc11	package	83291020008	derived:openfda.package_ndc
ndc11	package	83291020000	derived:openfda.package_ndc
ndc11	package	83291020052	derived:openfda.package_ndc
ndc11	package	83291020072	derived:openfda.package_ndc
ndc11	package	83291020004	derived:openfda.package_ndc
ndc11	package	83291020002	derived:openfda.package_ndc
rxcui		1603466	openfda.rxcui
rxcui		1188426	openfda.rxcui
spl id		7b0dddfc-9933-4f2f-840f-7a7b28cbf1fa	id
spl set id		b6966691-6884-438c-9f89-5924089226e1	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 Do not use is solution changes color or becomes cloudy. When using this product to avoid contamination, do not touch tip of container to any surface. Do not reuse. Once open, discard. do not touch unit dose tip to eye Stop use and ask a doctor before use 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.