REFRESH Optive Mega-3

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 Mega-3
Generic name: CARBOXYMETHYLCELLULOSE SODIUM, GLYCERIN AND POLYSORBATE 80
Manufacturer: Allergan, Inc.
Product type: HUMAN OTC DRUG
SPL set ID: c5f2b3f2-2071-45bd-a010-67f848bc0233
SPL ID: 4b93ea93-0dbb-4cb7-aae3-e48f04060bd1
Version: 9
Effective date: 2022-06-30
Source export date: 2026-10-27
Source partition: 12
Source file: https://download.open.fda.gov/drug/label/drug-label-0012-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-10-27/977776a6cc37ec1c77259da8a93ae161850a3aa120341096e5a03428b84d016b/drug-label-0012-of-0014.json.zip
Source manifest SHA-256: 6be3667a3beefe6c0ead4c723ea963050533a2bc725a8044d58b07d18b258c55
Import run: 20261027T193451Z
Imported at: 2026-10-27 21:00:43

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 Mega-3	openfda.brand_name
generic name		CARBOXYMETHYLCELLULOSE SODIUM, GLYCERIN AND POLYSORBATE 80	openfda.generic_name
manufacturer name		Allergan, Inc.	openfda.manufacturer_name
ndc	package	0023-5773-05	openfda.package_ndc
ndc	package	0023-5773-30	openfda.package_ndc
ndc	package	0023-4230-70	openfda.package_ndc
ndc	package	0023-7151-60	openfda.package_ndc
ndc	product	0023-5773	openfda.product_ndc
ndc	product	0023-7151	openfda.product_ndc
ndc	product	0023-4230	openfda.product_ndc
ndc11	package	00023577330	derived:openfda.package_ndc
ndc11	package	00023577305	derived:openfda.package_ndc
ndc11	package	00023715160	derived:openfda.package_ndc
ndc11	package	00023423070	derived:openfda.package_ndc
rxcui		1241471	openfda.rxcui
spl id		4b93ea93-0dbb-4cb7-aae3-e48f04060bd1	id
spl set id		c5f2b3f2-2071-45bd-a010-67f848bc0233	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. Do not reuse. Once opened, discard. Do not touch unit-dose tip to eye. 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.