Meijer Multi-Symptom Relief

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]

MEIJER MULTI-SYMPTOM RELIEF- polyethylene glycol, tetrahydrozoline hydrochloride, zinc sulfate solution/ drops 
K.C. Pharmaceuticals, Inc.

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

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Meijer Multi-Symptom Relief

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

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

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.

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 information

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

Inactive ingredients

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

Questions or comments?

Call 1-888-527-4276

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)

Revised: 1/2023

Document Id: f1a2bfe5-ef9f-92b7-e053-2995a90a4aa3

34390-5

Set id: f1a2bfe5-ef9e-92b7-e053-2995a90a4aa3

Version: 1

Effective Time: 20230106