SEASONAL ITCHY AND RED EYE RELIEF- tetrahydrozoline hcl, zinc sulfate liquid

Seasonal itchy and Red eye relief by

Drug Labeling and Warnings

Seasonal itchy and Red eye relief by is a Otc medication manufactured, distributed, or labeled by Kareway Product, Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient

Tetrahydrozoline HCl 0.05%

Zinc sulfate 0.25%

Purpose

Redness reliever

Astringent

Use

• for temporary relief of discomfort and redness of the eye due to minor eye irritations

Warnings

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 use if this solution changes color or become cloudy
• do not touch tip of container to any surface to avoid contamination
• replace cap after each use
  

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 right away.

Directions

• put 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

• store at 15° to 25°C (59° to 77°F)

Inactive ingredients

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

package label

INGREDIENTS AND APPEARANCE

SEASONAL ITCHY AND RED EYE RELIEF 
tetrahydrozoline hcl, zinc sulfate liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 67510-0665
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 mg  in 1 mL
ZINC SULFATE (UNII: 89DS0H96TB) (ZINC CATION - UNII:13S1S8SF37)	ZINC CATION	0.25 mg  in 1 mL

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

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 67510-0665-5	1 in 1 CARTON	11/12/2013
1		15 mL in 1 BOTTLE; Type 0: Not a Combination Product
2	NDC: 67510-0665-1	1 in 1 CARTON	11/12/2013
2		30 mL in 1 BOTTLE; 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	11/12/2013

Labeler - Kareway Product, Inc. (121840057)