REFRESH PLUS

Manufacturer: Allergan, Inc.
Effective date: 2022-06-28
Label type: HUMAN OTC DRUG LABEL
Version: 13
Source: daily-update
Hydrated at: 2026-08-04 03:32:54

Label at a glance#

ProductREFRESH PLUS

Active ingredientCARBOXYMETHYLCELLULOSE SODIUM

Label structure11 sections

Indications and uses

For the temporary relief of burning, irritation, and discomfort due to dryness of the eye or exposure to wind or sun. May be used as a protectant against further irritation.

Dosage and administration

To open, TWIST AND PULL TAB TO REMOVE . Instill 1 or 2 drops in the affected eye(s) as needed and discard container. *Follow your eye doctor’s instructions if you are using this product after an eye surgery (e.g., LASIK) to relieve eye dryness and discomfort.

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Carboxymethylcellulose sodium 0.5%

Purpose

OTC - PURPOSE SECTION

Eye lubricant

Uses

INDICATIONS & USAGE SECTION

For the temporary relief of burning, irritation, and discomfort due to dryness of the eye or exposure to wind or sun.
May be used as a protectant against further irritation.

Warnings

WARNINGS SECTION

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

OTC - STOP USE SECTION

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.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, get medical help or contact a Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

To open, TWIST AND PULL TAB TO REMOVE .

Instill 1 or 2 drops in the affected eye(s) as needed and discard container.

*Follow your eye doctor’s instructions if you are using this product after an eye surgery (e.g., LASIK) to relieve eye dryness and discomfort.

Other information

OTHER SAFETY INFORMATION

Use only if single-use container is intact.
Use before expiration date marked on container.
Store at 59°-77°F (15°-25°C).
RETAIN THIS CARTON FOR FUTURE REFERENCE.

Inactive ingredients

INACTIVE INGREDIENT SECTION

Calcium chloride dihydrate; magnesium chloride hexahydrate; potassium chloride; purified water; sodium chloride; and sodium lactate. May contain hydrochloric acid and/or sodium hydroxide (to adjust pH).

Questions or comments?

OTC - QUESTIONS SECTION

Phone icon1.800.678.1605

refresheyedrops.com

v2.0DFL0403

PRINCIPAL DISPLAY PANEL

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

NDC 0023-0403-30
P RESERVATIVE - FREE
Refresh
P LUS ®
Lubricant Eye Drops

Original Strength
Dry Eye Relief

30 Vials 0.01 fl oz (0.4 mL) each Sterile

PRINCIPAL DISPLAY PANEL NDC 0023-0403-30 PRESERVATIVE -FREE Refresh PLUS® Lubricant Eye Drops Original Strength Dry Eye Relief 30 Vials 0.01 fl oz (0.4 mL) each Sterile

PRINCIPAL DISPLAY PANEL

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

NDC 0023-0403-50
VALUE SIZE 50 Vials
PRESERVATIVE -FREE
Refresh
Plus®
Lubricant Eye Drops

Original Strength
Dry Eye Relief
50 Vials
0.01 fl oz (0.4 mL) each Sterile

PRINCIPAL DISPLAY PANEL NDC 0023-0403-50 VALUE SIZE 50 Vials PRESERVATIVE -FREE Refresh Plus® Lubricant Eye Drops Original Strength Dry Eye Relief 50 Vials 0.01 fl oz (0.4 mL) e...

PRINCIPAL DISPLAY PANEL

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

NDC 0023-0403-70
VALUE SIZE 70 Vials
PRESERVATIVE -FREE
Refresh
Plus ^®
Lubricant Eye Drops
Original Strength
Dry Eye Relief

70 Vials 0.01 fl oz (0.4mL) each Sterile

PRINCIPAL DISPLAY PANEL NDC 0023-0403-70 VALUE SIZE 70 Vials PRESERVATIVE -FREE Refresh Plus® Lubricant Eye Drops Original Strength Dry Eye Relief 70 Vials 0.01 fl oz (0.4mL) ea...

DailyMed Product Concepts#

Product concept, Relation, Version table
Product concept	Relation	Version	Effective
9e37788c-b1bf-42ae-aac9-b60601606144	Product name	8	20260122
30b0ac6e-02aa-0e5c-0d8b-cffdf3a282b2	Product name	5	20250304
1527ac37-808d-43be-a63e-74e1258dbe46	Product name	9	20250219
bed0530e-f939-4541-956b-6928a2f6404f	Product name	1	20241008
cefa60e2-a5b5-493e-9c54-24735b7dc509	Product name	6	20240814
362d7abb-94e6-4c60-9a58-266894157713	Product name	1	20231023
9fcb7a91-de07-4f00-aabf-e4d6fda403d5	Product name	8	20230322
6bd95106-a412-1dad-b9cc-4cb74bfb27ce	Product name	2	20230315
f1e0dc7e-7d61-4625-b6d9-4894927679d7	Product name	2	20211025
9badc7be-250a-44ab-aa36-926af3f02679	Product name	1	20210527
e4870509-7e28-6f92-f0be-dd3dd889a9cf	Product name	5	20200810
0ec3537a-6c9b-432a-896c-b9ea8723049a	Product name	9	20200701
6e9d4a47-c464-b93e-aebc-ad7bffc9c4cd	Product name	2	20190619
444b3e50-f226-46ef-bfca-2e7035d140cd	Product name	1	20190611
816b97af-edc5-4060-aff1-b814bdbcad50	Product name	1	20190415
7cda52fc-125f-421c-8fea-bc1974370c49	Product name	2	20180703
7916de40-e296-41f0-b811-6d0df1a33e2c	Product name	9	20180627
cefa60e2-a5b5-493e-9c54-24735b7dc509	Product name	2	20171212
419aab54-5d5a-4146-9453-026d4a9991be	Product name	2	20170525
d5e51f11-ad28-caa4-4b49-4143974782ad	Product name	1	20150831
290f523a-f9db-9774-b5a9-e1f908ac1782	Product name	1	20150828
0ca1d589-929b-4b33-bc5b-1d84abdafa6a	Product name	1	20150324
fc363c46-397b-4476-ac0f-70e43e8e4592	Product name	1	20150324
89dac932-b90a-4410-9ab1-84c53e57de25	Product name	1	20150316
5668b646-cd56-c3c7-bdea-3f6b1a8840db	Product name	1	20140508
597b1cfd-7b31-5048-62be-ca5cd740da2f	Product name	1	20140508
684ea482-2e8b-14af-5664-b98f1e402036	Product name	1	20140508
810ab97e-f109-f41c-7c83-6a652a9cbf43	Product name	1	20140508
87711080-88eb-65c5-b2dd-bf99e700a372	Product name	1	20140508
8dbefedf-0a0d-a224-5a3c-66dc9e11c2dd	Product name	1	20140508
b060cc1a-fe47-856b-0b77-4448b5963de8	Product name	1	20140508
c6b65c52-69c7-df49-550a-a50c137f6218	Product name	1	20140508
ec2149b3-5c6d-5344-f757-c86411073075	Product name	1	20140508
ed912195-5da0-0f2f-6f4b-3ef17710cbe3	Product name	1	20140508

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDC	Billing unit	Product NDC	DailyMed indexing SPL	SPL version	Effective
0023-0403-30	EA - Each	0023-0403	1b7dba73-1c21-4d6c-95c5-36b7766aa4cc	1	2012-07-24
0023-0403-50	EA - Each	0023-0403	20a7b344-7c02-4d09-b58e-5008980f2d82	1	2012-07-24
0023-0403-70	EA - Each	0023-0403	14e7ba33-8c0f-4406-a1fb-d69442f760da	1	2012-07-24

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	SPL version
carboxymethylcellulose sodium	ACTIVE INGREDIENT	K679OBS311	5
carboxymethylcellulose	ACTIVE MOIETY	05JZI7B19X	5
calcium chloride	INACTIVE INGREDIENT	M4I0D6VV5M	5
hydrochloric acid	INACTIVE INGREDIENT	QTT17582CB	5
magnesium chloride	INACTIVE INGREDIENT	02F3473H9O	5
potassium chloride	INACTIVE INGREDIENT	660YQ98I10	5
sodium chloride	INACTIVE INGREDIENT	451W47IQ8X	5
sodium hydroxide	INACTIVE INGREDIENT	55X04QC32I	5
sodium lactate	INACTIVE INGREDIENT	TU7HW0W0QT	5
water	INACTIVE INGREDIENT	059QF0KO0R	5

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 11 matching rows.

REFRESH PLUS
carboxymethylcellulose sodium
CARBOXYMETHYLCELLULOSE
CALCIUM CHLORIDE
MAGNESIUM CHLORIDE
POTASSIUM CHLORIDE
WATER
SODIUM CHLORIDE
SODIUM LACTATE
HYDROCHLORIC ACID
SODIUM HYDROXIDE

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
0023-0403	0023-0403-05, 0023-0403-30, 0023-0403-50, 0023-0403-70, 0023-0403-10

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 9 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
CARBOXYMETHYLCELLULOSE SODIUM	K679OBS311	ACTIB
CALCIUM CHLORIDE	M4I0D6VV5M	IACT
MAGNESIUM CHLORIDE	02F3473H9O	IACT
POTASSIUM CHLORIDE	660YQ98I10	IACT
WATER	059QF0KO0R	IACT
SODIUM CHLORIDE	451W47IQ8X	IACT
SODIUM LACTATE	TU7HW0W0QT	IACT
HYDROCHLORIC ACID	QTT17582CB	IACT
SODIUM HYDROXIDE	55X04QC32I	IACT

Source Document#

Source XML

Older Hydrated Versions#

Version, Effective date, Source table
Version	Effective date	Source	Hydrated
12	2022-06-28	full-release	2026-06-01 00:22:20

Inactive ingredient matches#

Inactive Ingredient Database values describe FDA-listed use contexts. The match method and ambiguity count are shown because ingredient names, routes, and dosage forms are not always unique. Browse recovered IID releases and source provenance.

Inactive ingredient links page 1 of 2 · 78 matching rows.

DailyMed ingredient, IID ingredient, UNII table
DailyMed ingredient	IID ingredient	UNII	Dosage form / route	Potency	Maximum daily exposure	Match
hydrochloric acid	HYDROCHLORIC ACID	QTT17582CB	SOLUTION/ DROPS / OPHTHALMIC	ADJ PH		Exact identifier — unii+route+dosage form 6 equally ranked IID candidates
sodium lactate	SODIUM LACTATE	TU7HW0W0QT	INJECTION, SOLUTION / INFILTRATION	0.17 %v/v		Exact identifier — unii candidate 42 equally ranked IID candidates
potassium chloride	POTASSIUM CHLORIDE	660YQ98I10	SOLUTION/ DROPS / OPHTHALMIC	0.14 %w/v		Exact identifier — unii+route+dosage form 6 equally ranked IID candidates
sodium lactate	SODIUM LACTATE	TU7HW0W0QT	SOLUTION / TOPICAL	0.93 %w/w		Exact identifier — unii candidate 42 equally ranked IID candidates
sodium lactate	SODIUM LACTATE	TU7HW0W0QT	INJECTION, SOLUTION / INFILTRATION	0.17 %v/v		Exact identifier — unii candidate 42 equally ranked IID candidates
sodium lactate	SODIUM LACTATE	TU7HW0W0QT	SOLUTION / TOPICAL	0.93 %w/w		Exact identifier — unii candidate 42 equally ranked IID candidates
sodium lactate	SODIUM LACTATE	TU7HW0W0QT	INJECTION, SOLUTION / INFILTRATION	0.17 %v/v		Exact identifier — unii candidate 42 equally ranked IID candidates
sodium chloride	SODIUM CHLORIDE	451W47IQ8X	SOLUTION/ DROPS / OPHTHALMIC		55 mg	Exact identifier — unii+route+dosage form 6 equally ranked IID candidates
sodium hydroxide	SODIUM HYDROXIDE	55X04QC32I	SOLUTION/ DROPS / OPHTHALMIC	ADJ PH		Exact identifier — unii+route+dosage form 6 equally ranked IID candidates
sodium lactate	SODIUM LACTATE	TU7HW0W0QT	INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION / INTRAVENOUS	18.7 mg		Exact identifier — unii candidate 42 equally ranked IID candidates
sodium lactate	SODIUM LACTATE	TU7HW0W0QT	INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION / INTRAVENOUS	18.7 mg		Exact identifier — unii candidate 42 equally ranked IID candidates
sodium lactate	SODIUM LACTATE	TU7HW0W0QT	SOLUTION / INTRAPERITONEAL	0.45 %w/v		Exact identifier — unii candidate 42 equally ranked IID candidates
sodium lactate	SODIUM LACTATE	TU7HW0W0QT	INJECTION / INTRAVENOUS		54 mg	Exact identifier — unii candidate 42 equally ranked IID candidates
sodium lactate	SODIUM LACTATE	TU7HW0W0QT	SOLUTION / INTRAPERITONEAL	0.45 %w/v		Exact identifier — unii candidate 42 equally ranked IID candidates
hydrochloric acid	HYDROCHLORIC ACID	QTT17582CB	SOLUTION/ DROPS / OPHTHALMIC	ADJ PH		Exact identifier — unii+route+dosage form 6 equally ranked IID candidates
sodium lactate	SODIUM LACTATE	TU7HW0W0QT	GEL / TOPICAL		4 mg	Exact identifier — unii candidate 42 equally ranked IID candidates
sodium lactate	SODIUM LACTATE	TU7HW0W0QT	GEL / TOPICAL		4 mg	Exact identifier — unii candidate 42 equally ranked IID candidates
sodium lactate	SODIUM LACTATE	TU7HW0W0QT	SOLUTION / TOPICAL	0.93 %w/w		Exact identifier — unii candidate 42 equally ranked IID candidates
sodium hydroxide	SODIUM HYDROXIDE	55X04QC32I	SOLUTION/ DROPS / OPHTHALMIC	ADJ PH		Exact identifier — unii+route+dosage form 6 equally ranked IID candidates
potassium chloride	POTASSIUM CHLORIDE	660YQ98I10	SOLUTION/ DROPS / OPHTHALMIC	0.14 %w/v		Exact identifier — unii+route+dosage form 6 equally ranked IID candidates
sodium chloride	SODIUM CHLORIDE	451W47IQ8X	SOLUTION/ DROPS / OPHTHALMIC		55 mg	Exact identifier — unii+route+dosage form 6 equally ranked IID candidates
sodium hydroxide	SODIUM HYDROXIDE	55X04QC32I	SOLUTION/ DROPS / OPHTHALMIC	ADJ PH		Exact identifier — unii+route+dosage form 6 equally ranked IID candidates
magnesium chloride	MAGNESIUM CHLORIDE	02F3473H9O	SOLUTION/ DROPS / OPHTHALMIC	0.03 %w/v		Exact identifier — unii+route+dosage form 6 equally ranked IID candidates
calcium chloride	CALCIUM CHLORIDE	M4I0D6VV5M	SOLUTION/ DROPS / OPHTHALMIC	0.02 %w/v		Exact identifier — unii+route+dosage form 6 equally ranked IID candidates
potassium chloride	POTASSIUM CHLORIDE	660YQ98I10	SOLUTION/ DROPS / OPHTHALMIC	0.14 %w/v		Exact identifier — unii+route+dosage form 6 equally ranked IID candidates
calcium chloride	CALCIUM CHLORIDE	M4I0D6VV5M	SOLUTION/ DROPS / OPHTHALMIC	0.02 %w/v		Exact identifier — unii+route+dosage form 6 equally ranked IID candidates
potassium chloride	POTASSIUM CHLORIDE	660YQ98I10	SOLUTION/ DROPS / OPHTHALMIC	0.14 %w/v		Exact identifier — unii+route+dosage form 6 equally ranked IID candidates
calcium chloride	CALCIUM CHLORIDE	M4I0D6VV5M	SOLUTION/ DROPS / OPHTHALMIC	0.02 %w/v		Exact identifier — unii+route+dosage form 6 equally ranked IID candidates
magnesium chloride	MAGNESIUM CHLORIDE	02F3473H9O	SOLUTION/ DROPS / OPHTHALMIC	0.03 %w/v		Exact identifier — unii+route+dosage form 6 equally ranked IID candidates
hydrochloric acid	HYDROCHLORIC ACID	QTT17582CB	SOLUTION/ DROPS / OPHTHALMIC	ADJ PH		Exact identifier — unii+route+dosage form 6 equally ranked IID candidates
sodium hydroxide	SODIUM HYDROXIDE	55X04QC32I	SOLUTION/ DROPS / OPHTHALMIC	ADJ PH		Exact identifier — unii+route+dosage form 6 equally ranked IID candidates
magnesium chloride	MAGNESIUM CHLORIDE	02F3473H9O	SOLUTION/ DROPS / OPHTHALMIC	0.03 %w/v		Exact identifier — unii+route+dosage form 6 equally ranked IID candidates
magnesium chloride	MAGNESIUM CHLORIDE	02F3473H9O	SOLUTION/ DROPS / OPHTHALMIC	0.03 %w/v		Exact identifier — unii+route+dosage form 6 equally ranked IID candidates
sodium lactate	SODIUM LACTATE	TU7HW0W0QT	SOLUTION / TOPICAL	0.93 %w/w		Exact identifier — unii candidate 42 equally ranked IID candidates
magnesium chloride	MAGNESIUM CHLORIDE	02F3473H9O	SOLUTION/ DROPS / OPHTHALMIC	0.03 %w/v		Exact identifier — unii+route+dosage form 6 equally ranked IID candidates
sodium lactate	SODIUM LACTATE	TU7HW0W0QT	SUSPENSION / ORAL	20 mg/1ml		Exact identifier — unii candidate 42 equally ranked IID candidates
sodium lactate	SODIUM LACTATE	TU7HW0W0QT	INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION / INTRAVENOUS	18.7 mg		Exact identifier — unii candidate 42 equally ranked IID candidates
sodium lactate	SODIUM LACTATE	TU7HW0W0QT	GEL / TOPICAL		4 mg	Exact identifier — unii candidate 42 equally ranked IID candidates
sodium lactate	SODIUM LACTATE	TU7HW0W0QT	INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION / INTRAVENOUS	18.7 mg		Exact identifier — unii candidate 42 equally ranked IID candidates
sodium lactate	SODIUM LACTATE	TU7HW0W0QT	INJECTION / INTRAVENOUS		54 mg	Exact identifier — unii candidate 42 equally ranked IID candidates
sodium lactate	SODIUM LACTATE	TU7HW0W0QT	GEL / TOPICAL		4 mg	Exact identifier — unii candidate 42 equally ranked IID candidates
sodium lactate	SODIUM LACTATE	TU7HW0W0QT	INJECTION, SOLUTION / INFILTRATION	0.17 %v/v		Exact identifier — unii candidate 42 equally ranked IID candidates
sodium lactate	SODIUM LACTATE	TU7HW0W0QT	INJECTION, SOLUTION / INFILTRATION	0.17 %v/v		Exact identifier — unii candidate 42 equally ranked IID candidates
sodium lactate	SODIUM LACTATE	TU7HW0W0QT	INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION / INTRAVENOUS	18.7 mg		Exact identifier — unii candidate 42 equally ranked IID candidates
hydrochloric acid	HYDROCHLORIC ACID	QTT17582CB	SOLUTION/ DROPS / OPHTHALMIC	ADJ PH		Exact identifier — unii+route+dosage form 6 equally ranked IID candidates
sodium hydroxide	SODIUM HYDROXIDE	55X04QC32I	SOLUTION/ DROPS / OPHTHALMIC	ADJ PH		Exact identifier — unii+route+dosage form 6 equally ranked IID candidates
hydrochloric acid	HYDROCHLORIC ACID	QTT17582CB	SOLUTION/ DROPS / OPHTHALMIC	ADJ PH		Exact identifier — unii+route+dosage form 6 equally ranked IID candidates
sodium chloride	SODIUM CHLORIDE	451W47IQ8X	SOLUTION/ DROPS / OPHTHALMIC		55 mg	Exact identifier — unii+route+dosage form 6 equally ranked IID candidates
calcium chloride	CALCIUM CHLORIDE	M4I0D6VV5M	SOLUTION/ DROPS / OPHTHALMIC	0.02 %w/v		Exact identifier — unii+route+dosage form 6 equally ranked IID candidates
sodium lactate	SODIUM LACTATE	TU7HW0W0QT	SOLUTION / INTRAPERITONEAL	0.45 %w/v		Exact identifier — unii candidate 42 equally ranked IID candidates
sodium lactate	SODIUM LACTATE	TU7HW0W0QT	SUSPENSION / ORAL	20 mg/1ml		Exact identifier — unii candidate 42 equally ranked IID candidates
potassium chloride	POTASSIUM CHLORIDE	660YQ98I10	SOLUTION/ DROPS / OPHTHALMIC	0.14 %w/v		Exact identifier — unii+route+dosage form 6 equally ranked IID candidates
sodium lactate	SODIUM LACTATE	TU7HW0W0QT	INJECTION / INTRAVENOUS		54 mg	Exact identifier — unii candidate 42 equally ranked IID candidates
sodium lactate	SODIUM LACTATE	TU7HW0W0QT	GEL / TOPICAL		4 mg	Exact identifier — unii candidate 42 equally ranked IID candidates
sodium lactate	SODIUM LACTATE	TU7HW0W0QT	SUSPENSION / ORAL	20 mg/1ml		Exact identifier — unii candidate 42 equally ranked IID candidates
magnesium chloride	MAGNESIUM CHLORIDE	02F3473H9O	SOLUTION/ DROPS / OPHTHALMIC	0.03 %w/v		Exact identifier — unii+route+dosage form 6 equally ranked IID candidates
sodium chloride	SODIUM CHLORIDE	451W47IQ8X	SOLUTION/ DROPS / OPHTHALMIC		55 mg	Exact identifier — unii+route+dosage form 6 equally ranked IID candidates
sodium lactate	SODIUM LACTATE	TU7HW0W0QT	INJECTION / INTRAVENOUS		54 mg	Exact identifier — unii candidate 42 equally ranked IID candidates
sodium lactate	SODIUM LACTATE	TU7HW0W0QT	INJECTION / INTRAVENOUS		54 mg	Exact identifier — unii candidate 42 equally ranked IID candidates
sodium lactate	SODIUM LACTATE	TU7HW0W0QT	SOLUTION / TOPICAL	0.93 %w/w		Exact identifier — unii candidate 42 equally ranked IID candidates

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 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
REFRESH PLUS	CARBOXYMETHYLCELLULOSE SODIUM	Allergan, Inc.	0f6a4b4b-cde6-4518-84b5-ce997f1154a7	2022-06-28	Warnings	Exact identifier ndc (package): 0023-0403-50 ndc (package): 0023-0403-70 ndc (package): 0023-0403-30 ndc (package): 0023-0403-05 ndc (package): 0023-0403-10 ndc (product): 0023-0403 ndc11 (package): 00023040350 ndc11 (package): 00023040305 ndc11 (package): 00023040310 ndc11 (package): 00023040370 ndc11 (package): 00023040330 spl id: 35d7ddb8-a31b-4cd3-a0c5-f06fa13f38fa spl set id: 0f6a4b4b-cde6-4518-84b5-ce997f1154a7

Reported adverse events (FAERS/openFDA)#

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