Meijer Multi-Symptom Relief

Manufacturer
K.C. Pharmaceuticals, Inc.
Effective date
2023-01-06
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 21:41:24

Label at a glance#

ProductMeijer Multi-Symptom Relief
Active ingredientTETRAHYDROZOLINE HYDROCHLORIDE, POLYETHYLENE GLYCOL 400, ZINC SULFATE
Label structure8 sections

Label contents#

Full prescribing information#

DRUG FACTS

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 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 - ASK DOCTOR 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 20-25°C (68-77ºF)

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

Products#

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NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
55651-25055651-250-01

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
f1a2bfe5-ef9f-92b7-e053-2995a90a4aa3f1a2bfe5-ef9e-92b7-e053-2995a90a4aa32023-01-06WarningsExact identifier
spl id: f1a2bfe5-ef9f-92b7-e053-2995a90a4aa3
spl set id: f1a2bfe5-ef9e-92b7-e053-2995a90a4aa3

Reported adverse events (FAERS/openFDA)#

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