REFRESH OPTIVE Advanced

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: REFRESH OPTIVE Advanced
Generic name: CARBOXYMETHYLCELLULOSE SODIUM, GLYCERIN, AND POLYSORBATE 80
Manufacturer: Allergan, Inc.
Product type: HUMAN OTC DRUG
SPL set ID: aaa943e4-7c38-4c5a-b7c0-5a656d8cafc0
SPL ID: 82284b10-2578-4490-bb19-e38da030a102
Version: 16
Effective date: 2022-09-01
Source export date: 2026-09-28
Source partition: 11
Source file: https://download.open.fda.gov/drug/label/drug-label-0011-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-09-28/aa96b5a2be6b394393acd0090f6948bdf99e0e8e00666f81608929c8fa83db77/drug-label-0011-of-0014.json.zip
Source manifest SHA-256: cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run: 20260929T050834Z
Imported at: 2026-09-29 06:16:46

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 · 21 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		M018	openfda.application_number
brand name		REFRESH OPTIVE Advanced	openfda.brand_name
generic name		CARBOXYMETHYLCELLULOSE SODIUM, GLYCERIN, AND POLYSORBATE 80	openfda.generic_name
manufacturer name		Allergan, Inc.	openfda.manufacturer_name
ndc	package	0023-4307-10	openfda.package_ndc
ndc	package	0023-4307-15	openfda.package_ndc
ndc	package	0023-4307-20	openfda.package_ndc
ndc	package	0023-4307-03	openfda.package_ndc
ndc	package	0023-4307-02	openfda.package_ndc
ndc	product	0023-4307	openfda.product_ndc
ndc11	package	00023430703	derived:openfda.package_ndc
ndc11	package	00023430715	derived:openfda.package_ndc
ndc11	package	00023430720	derived:openfda.package_ndc
ndc11	package	00023430710	derived:openfda.package_ndc
ndc11	package	00023430702	derived:openfda.package_ndc
rxcui		1241471	openfda.rxcui
spl id		82284b10-2578-4490-bb19-e38da030a102	id
spl set id		aaa943e4-7c38-4c5a-b7c0-5a656d8cafc0	set_id
unii		PDC6A3C0OX	openfda.unii
unii		6OZP39ZG8H	openfda.unii
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. Replace cap after using. If solution changes color, 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.