ORIGINAL REDNESS RELIEVER- tetrahydrolizine hcl solution/ drops

Original Redness Reliever by

Drug Labeling and Warnings

Original Redness Reliever by is a Otc medication manufactured, distributed, or labeled by Walmart. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Purpose

Redness Reliever

ACTIVE INGREDIENT

Active ingredient
TetrahydrozolineHCI0.05%

KEEP OUT OF REACH OF CHILDREN

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center
(1-800-222-1222) right away.

INACTIVE INGREDIENT

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

DOSAGE & ADMINISTRATION

Directions
instill 1 to 2 drops in the affected eye(s) up to 4times daily

INDICATIONS & USAGE

■ relieves redness of the eye due to minor eye irritations

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
■ to avoid contamination, do not touch tip of container to any surface. Replace cap after using.
■ if solution changes color or becomes cloudy, do not use
■ overuse may produce increased redness of the eye
■ remove contact lenses before using
Stop use and ask a doctor if you experience
■ eye pain
■ changes in vision
■ continued redness or irritation of the eye, or if the condition worsens or persists for more
than 72 hours
Hpregnant orbreast-feeding,askahealth professional before use.

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

ORIGINAL REDNESS RELIEVER 
tetrahydrolizine hcl solution/ drops

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 79903-363
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

Inactive Ingredients
Ingredient Name	Strength
SODIUM CHLORIDE (UNII: 451W47IQ8X)
SODIUM BORATE (UNII: 91MBZ8H3QO)
WATER (UNII: 059QF0KO0R)
EDETATE DISODIUM (UNII: 7FLD91C86K)
BORIC ACID (UNII: R57ZHV85D4)
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 79903-363-01	1 in 1 BOX	12/26/2025
1		15 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 Drug	M018	12/26/2025

Labeler - Walmart (051957769)