REDNESS AND DRY EYE RELIEF- glycerin, naphazoline hydrochloride solution

Redness and Dry Eye Relief by

Drug Labeling and Warnings

Redness and Dry Eye Relief by is a Otc medication manufactured, distributed, or labeled by KC Pharmaceuticals, Inc. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Active ingredients
Glycerin 0.25%
Naphazoline HCI 0.012%

PURPOSE

Active ingredients Purposes
Glycerin 0.25%........................................................Lubricant
Naphazoline HCI 0.012%........................................Redness reliever

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 Ingredients

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

DOSAGE & ADMINISTRATION

Directions:
instill 1 to 2 drops Ianthe affected eye(s) up to 4 times daily

INDICATIONS & USAGE

Uses
■ relieves redness of the eye due to minor eye irritations
■ for use as a protectant against further irritation or to relieve dryness of the eye
■ for the temporary relief of burning and irritation due to dryness of the eye

WARNINGS

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

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

REDNESS AND DRY EYE RELIEF 
glycerin, naphazoline hydrochloride solution

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 55651-620
Route of Administration	OPHTHALMIC

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
GLYCERIN (UNII: PDC6A3C0OX) (GLYCERIN - UNII:PDC6A3C0OX)	GLYCERIN	0.25 g  in 100 mL
NAPHAZOLINE HYDROCHLORIDE (UNII: MZ1131787D) (NAPHAZOLINE - UNII:H231GF11BV)	NAPHAZOLINE HYDROCHLORIDE	0.012 g  in 100 mL

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

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 55651-620-01	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 - KC Pharmaceuticals, Inc (174450460)