EQUATE REDNESS RELIEVER- tetrahydrozoline hydrochloride solution/ drops

Equate Redness Reliever by

Drug Labeling and Warnings

Equate Redness Reliever by is a Otc medication manufactured, distributed, or labeled by WALMART INC.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

SPL UNCLASSIFIED SECTION

Drug Facts

Active ingredient

Tetrahydrozoline Hydrochloride 0.05%

Purpose

Redness reliever

Uses

• relieves redness of the eye due to minor eye irritations

Warnings

For external use only

Do not use

• if solution changes color or becomes cloudy

Ask a doctor before use if you have

• narrow angle glaucoma

When using this product

• to avoid contamination, do not touch tip of container to any surface
  
• replace cap after using
  
• overuse may produce increased redness of the eye
  
• pupils may become enlarged temporarily

Stop use and ask a doctor if

• you experience eye pain
  
• you experience changes in vision
  
• you experience continued redness or irritation of the eye
  
• the condition worsens or persists for more than 72 hours

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 four times daily

Other information

• store at room temperature
  
• remove contact lenses before using

Inactive ingredients

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

Questions?

1-888-287-1915

Principal Display Panel

Equate®
Original Redness Reliever
Tetrahydrozoline HCI
Sterile Eye Drops
1 FL OZ (30 mL)

Principal Display Panel

Equate®
Original Redness
Reliever
Tetrahydrozoline HCI
Sterile Eye Drops
0.5 FL OZ (15 mL)

INGREDIENTS AND APPEARANCE

EQUATE REDNESS RELIEVER 
tetrahydrozoline hydrochloride solution/ drops

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 79903-010
Route of Administration	OPHTHALMIC

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
TETRAHYDROZOLINE HYDROCHLORIDE (UNII: 0YZT43HS7D) (TETRAHYDROZOLINE - UNII:S9U025Y077)	TETRAHYDROZOLINE HYDROCHLORIDE	0.5 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7)
BORIC ACID (UNII: R57ZHV85D4)
EDETATE DISODIUM (UNII: 7FLD91C86K)
WATER (UNII: 059QF0KO0R)
SODIUM BORATE (UNII: 91MBZ8H3QO)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 79903-010-15	1 in 1 CARTON	04/26/2013
1		15 mL in 1 BOTTLE; Type 0: Not a Combination Product
2	NDC: 79903-010-30	1 in 1 CARTON	04/26/2013
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	04/26/2013

Labeler - WALMART INC. (051957769)