FDA.reportPublic FDA data

Meijer Multi-Symptom Relief

Manufacturer
Meijer, Inc. | K.C. Pharmaceuticals, Inc.
Effective date
2025-12-30
Label type
HUMAN OTC DRUG LABEL
Version
4
Source
full-release
Hydrated at
2026-06-01 01:30:45

Label at a glance#

ProductMeijer Multi-Symptom Relief
Active ingredientTETRAHYDROZOLINE HYDROCHLORIDE, ZINC SULFATE, POLYETHYLENE GLYCOL 400
Label structure9 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active ingredients

Polyethylene glycol 400....1%

Tetrahydrozoline HCl .......0.05%

Zinc sulfate.......................0.25%

OTC - PURPOSE SECTION

Purposes

Polyethylene glycol 400 ......Lubricant

Tetrahydrozoline HCl ..........Redness reliever

Zinc sulfate .........................Astringent

INDICATIONS & USAGE SECTION

Uses

  • Relieves dryness of the eye
  • for temporary relief of discomfort and redness of the eye due to minor eye irritations
  • 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 lip 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, glycerin, hypromellose, purified water, sodium chloride, sodium citrate

OTC - QUESTIONS SECTION

Questions or comments?

Call 1-888-527-4276

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

CartonCarton

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
2360903polyethylene glycol 400 1 % / tetrahydrozoline hydrochloride 0.05 % / zinc sulfate 0.25 % Ophthalmic SolutionPSN4
2360903polyethylene glycol 400 10 MG/ML / tetrahydrozoline hydrochloride 0.5 MG/ML / zinc sulfate 2.5 MG/ML Ophthalmic SolutionSCD4
2360903polyethylene glycol 400 1 % / tetrahydrozoline hydrochloride 0.05 % / zinc sulfate 0.25 % Ophthalmic SolutionSY4
2360903polyethylene glycol 400 10 MG/ML / tetrahydrozoline hydrochloride 0.5 MG/ML / ZnSO4 2.5 MG/ML Ophthalmic SolutionSY4

DailyMed Pharmacologic Classes#

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

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
BarcodeEAN-130713733201391GTIN-13: 0713733201391
EAN-13: 0713733201391
GTIN-12: 713733201391
UPC-A: 713733201391
GTIN storage (14 digits): 00713733201391		MeijerMultiSymptom.jpg

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
27945931-b6e2-158e-d615-4ef21e2af974Product name120140508

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
79481-0250-1Meijer Multi-Symptom Relief15 mL in 1 BOTTLE, DROPPERSOLUTION/ DROPS154
79481-0250-1Meijer Multi-Symptom Relief1 in 1 CARTONSOLUTION/ DROPS14

Products#

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

DailyMed product names page 1 of 1 · 15 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
79481-025079481-0250-1

Ingredients#

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

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

Name, UNII, Kind table
NameUNIIKind
TETRAHYDROZOLINE HYDROCHLORIDE0YZT43HS7DACTIB
ZINC SULFATE89DS0H96TBACTIB
BORIC ACIDR57ZHV85D4IACT
GLYCERINPDC6A3C0OXIACT
WATER059QF0KO0RIACT
BENZALKONIUM CHLORIDEF5UM2KM3W7IACT
SODIUM CHLORIDE451W47IQ8XIACT
SODIUM CITRATE1Q73Q2JULRIACT
EDETATE DISODIUM7FLD91C86KIACT
HYPROMELLOSES3NXW29V3WOIACT
POLYETHYLENE GLYCOL 400B697894SGQACTIB

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
Meijer Multi-Symptom ReliefPOLYETHYLENE GLYCOL 400, TETRAHYDROZOLINE HCL, ZINC SULFATEMeijer, Inc.e7a5677a-ff33-c039-e053-2a95a90ae6c72025-12-30WarningsExact identifier
ndc (package): 79481-0250-1
ndc (product): 79481-0250
ndc11 (package): 79481025001
spl id: 474935fe-0614-4bfc-e063-6294a90ab6b2
spl set id: e7a5677a-ff33-c039-e053-2a95a90ae6c7

Reported adverse events (FAERS/openFDA)#

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