Walgreens Multi-Symptom Relief Eye Drops

Manufacturer
Walgreen Co. | K.C. Pharmaceuticals, Inc.
Effective date
2023-12-20
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-06-01 00:05:13

Label at a glance#

ProductWalgreens Multi-Symptom Relief Eye Drops
Active ingredientHYPROMELLOSE, UNSPECIFIED, POLYETHYLENE GLYCOL 400, ZINC SULFATE, GLYCERIN, TETRAHYDROZOLINE HYDROCHLORIDE
Label structure10 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active ingredients

Glycerin ....0.2%

Hypromellose.....0.36%

Polyethylene glycol 400.....1%

Tetrahydrozoline HCl.....0.05%

Zinc sulfate 0.25%

OTC - PURPOSE SECTION

Purposes

Glycerin ....Lubricant

Hypromellose.....Lubricant

Polyethylene glycol 400.....Lubricant

Tetrahydrozoline HCl.....Redness reliever

Zinc sulfate.....Astringent

INDICATIONS & USAGE SECTION

Uses

  • for temporary relief of discomfort and redness of the eye due to minor eye irritations
  • relieves dryness of the eye
  • for temporary relief of burning and irritation due to exposure to wind or sun
  • for protection against further irritation

OTC - PURPOSE SECTION

​Uses

  • for temporary relief of discomfort and redness of the eye due to minor eye irritations
  • relieves dryness of the eye
  • for temporary relief of burning and irritation due to exposure to wind or sun
  • for protection against further irritation

WARNINGS SECTION

Warnings

For external use only

OTC - ASK DOCTOR SECTION

Ask a doctor before use if you have narrow angle glaucoma

OTC - WHEN USING SECTION

When using this product

  • pupils may become enlarged temporarily
  • overuse may cause more eye redness
  • remove contact lenses before using
  • do not touch tip of container to any surface to avoid contamination
  • replace cap after using
  • do not use if this solution changes color or becomes cloudy

OTC - STOP USE SECTION

Stop use and ask a doctor if

  • you feel eye pain
  • changes in vision occur
  • redness or irritation of the eye lasts
  • condition worsens or lasts more than 72 hours

OTC - PREGNANCY OR BREAST FEEDING SECTION

If pregnant or breast-feeding, ask a health professional before use.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center (1-800-222-1222) right away.

DOSAGE & ADMINISTRATION SECTION

Directions

  • instill 1 to 2 drops in the affected eye(s) up to 4 times daily
  • children under 6 years of age: ask a doctor

OTHER SAFETY INFORMATION

Other information

  • some users may experience a brief tingling sensation
  • store at 20º-25ºC (68º-77ºF)

INACTIVE INGREDIENT SECTION

Inactive ingredients

  • benzalkonium chloride, boric acid, edetate disodium, purified water, sodium chloride, sodium citrate

OTC - QUESTIONS SECTION

Questions or comments?

1-888-527-4276

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

cartoncarton

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1148249glycerin 0.2 % / hypromellose 0.36 % / polyethylene glycol 400 1 % / tetrahydrozoline HCl 0.05 % / zinc sulfate 0.25 % Ophthalmic SolutionPSN2
1148249glycerin 2 MG/ML / hypromellose 3.6 MG/ML / polyethylene glycol 400 10 MG/ML / tetrahydrozoline hydrochloride 0.5 MG/ML / zinc sulfate 2.5 MG/ML Ophthalmic SolutionSCD2
1148249glycerin 0.2 % / hypromellose 0.36 % / polyethylene glycol 400 1 % / tetrahydrozoline HCl 0.05 % / zinc sulfate 0.25 % Ophthalmic SolutionSY2
1148249Glycerin 2 MG/ML / hypromellose 3.6 MG/ML / Polyethylene Glycol 400 10 MG/ML / Tetrahydrozoline hydrochloride 0.5 MG/ML / ZnSO4 2.5 MG/ML Ophthalmic SolutionSY2

DailyMed Pharmacologic Classes#

Class, Version, Type table
ClassVersionTypeEffective
GLYCERIN Pharmacologic Class Indexing2Indexing - Pharmacologic Class20180813
ZINC CATION Pharmacologic Class Indexing2Indexing - Pharmacologic Class20180813

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
f47a510b-6679-4664-b2d6-47b5c4afe7ccProduct name420260217
030ce964-9b2d-45aa-b5d3-f78ce03ef61cProduct name220250515
777d68c6-a5ab-e06c-d314-677b0b9af0c8Product name220240508
0306390c-dd77-4363-afe0-63c58088b2a1Product name120220120
503ea967-4b9c-48cf-9e87-c7975295849dProduct name220220120
190f2a5b-bbc8-65c7-fcb0-97891307b917Product name120140508
27945931-b6e2-158e-d615-4ef21e2af974Product name120140508

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
0363-1462-01Walgreens Multi-Symptom Relief Eye Drops15 mL in 1 BOTTLE, DROPPERSOLUTION/ DROPS152
0363-1462-01Walgreens Multi-Symptom Relief Eye Drops1 in 1 CARTONSOLUTION/ DROPS12

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
0363-1462WALGREENS MULTI-SYMPTOM RELIEF EYE DROPS (GLYCERIN, HYPROMELLOSE, POLYETHYLENE GLYCOL 400, TETRAHYDROZOLINE HCL, ZINC SULFATE) SOLUTION/ DROPS [WALGREEN CO.]2Current NDC, Legacy NDC, 2 package rows20231221_a03789ce-66bd-7b12-e053-2995a90af85a.zip

Products#

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

DailyMed product names page 1 of 1 · 16 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
0363-14620363-1462-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 11 matching rows.

Source Document#

Source XML

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
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Walgreens Multi-Symptom Relief Eye DropsGLYCERIN, HYPROMELLOSE, POLYETHYLENE GLYCOL 400, TETRAHYDROZOLINE HCL, ZINC SULFATEWalgreen Co.a03789ce-66bd-7b12-e053-2995a90af85a2023-12-20WarningsExact identifier
ndc (package): 0363-1462-01
ndc (product): 0363-1462
ndc11 (package): 00363146201
spl id: 0cf9613b-2fae-88c0-e063-6394a90adac9
spl set id: a03789ce-66bd-7b12-e053-2995a90af85a

Reported adverse events (FAERS/openFDA)#

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