MEIJER MULTI-SYMPTOM RELIEF- polyethylene glycol, tetrahydrozoline hydrochloride, zinc sulfate solution/ drops

Meijer Multi-Symptom Relief by

Drug Labeling and Warnings

Meijer Multi-Symptom Relief by is a Otc medication manufactured, distributed, or labeled by K.C. Pharmaceuticals, Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

DRUG FACTS

Active ingredients

Polyethylene glycol 400 ........1%

Tetrahydrozoline HCl.............0.05%

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

Purposes

Polyethylene glycol 400 .....Lubricant

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

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

INDICATIONS & USAGE

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

Warnings

For external use only

Ask a doctor before use if you have narrow angle glaucoma

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

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

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

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

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

Inactive ingredients

benzalkonium chloride, boric acid, edetate disodium, glycerin, hypromellose, purified water, sodium chloride, sodium citrate

QUESTIONS

Questions or comments?

Call 1-888-527-4276

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

MEIJER MULTI-SYMPTOM RELIEF 
polyethylene glycol, tetrahydrozoline hydrochloride, zinc sulfate solution/ drops

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 55651-250
Route of Administration	OPHTHALMIC

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
TETRAHYDROZOLINE HYDROCHLORIDE (UNII: 0YZT43HS7D) (TETRAHYDROZOLINE - UNII:S9U025Y077)	TETRAHYDROZOLINE HYDROCHLORIDE	0.05 g  in 100 mL
POLYETHYLENE GLYCOL 400 (UNII: B697894SGQ) (POLYETHYLENE GLYCOL 400 - UNII:B697894SGQ)	POLYETHYLENE GLYCOL 400	1 g  in 100 mL
ZINC SULFATE (UNII: 89DS0H96TB) (ZINC CATION - UNII:13S1S8SF37)	ZINC SULFATE	0.25 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
SODIUM CITRATE (UNII: 1Q73Q2JULR)
BORIC ACID (UNII: R57ZHV85D4)
GLYCERIN (UNII: PDC6A3C0OX)
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7)
EDETATE DISODIUM (UNII: 7FLD91C86K)
HYPROMELLOSES (UNII: 3NXW29V3WO)
SODIUM CHLORIDE (UNII: 451W47IQ8X)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 55651-250-01	1 in 1 CARTON	01/09/2023
1		15 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part349	01/09/2023

Labeler - K.C. Pharmaceuticals, Inc. (174450460)

Establishment
Name	Address	ID/FEI	Business Operations
K.C. Pharmaceuticals, Inc.		174450460	manufacture(55651-250) , pack(55651-250) , label(55651-250)