ADVANCED EYE RELIEF/ REDNESS MAXIMUM RELIEF- naphazoline hydrochloride and hypromellose solution/ drops

Advanced Eye Relief/ Redness Maximum Relief by

Drug Labeling and Warnings

Advanced Eye Relief/ Redness Maximum Relief by is a Otc medication manufactured, distributed, or labeled by Preferred Pharmaceuticals Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active ingredients

Hypromellose (0.5%)

Naphazoline hydrochloride (0.03%)

Purpose

Lubricant

Redness reliever

Uses

• temporary relief of redness and discomfort due to:
  • minor eye irritations
  • exposure to wind or sun
  • dryness of the eye
• prevents further irritation

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

• do not touch tip of container to any surface to avoid contamination
• do not overuse as it may produce increased redness of the eye
• pupils may become enlarged temporarily
• remove contact lenses before using
• replace cap after use

Stop use and ask a doctor if

• you experience eye pain, changes in vision, continued redness or irritation of the eye
• 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 right away.

Directions

• instill 1 to 2 drops in the affected eye(s) up to four times daily

Other information

• store at 15°-25°C (59°-77°F)
• keep tightly closed
• use before expiration date marked on the carton and bottle

Inactive ingredients

benzalkonium chloride (0.01%), boric acid, edetate disodium, purified water, sodium borate, sodium chloride. Hydrochloric acid and/or sodium hydroxide may be used to adjust pH.

Questions or comments?

[phone icon] Call: 1-800-553-5340

Package/Label Principal Display Panel

NEW LOOK! same formula

BAUSCH + LOMB

ADVANCED

Eye Relief®

Maximum

Redness

REDNESS RELIEVER/

LUBRICANT EYE DROPS

• Maximum strength
•   redness reliever
• Moisturizes and
•   comforts

STERILE 0.5 FL OZ (15mL)

Relabeled By: Preferred Pharmaceuticals Inc.

INGREDIENTS AND APPEARANCE

ADVANCED EYE RELIEF/ REDNESS MAXIMUM RELIEF 
naphazoline hydrochloride and hypromellose solution/ drops

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 68788-6973(NDC:24208-450)
Route of Administration	OPHTHALMIC

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
HYPROMELLOSE, UNSPECIFIED (UNII: 3NXW29V3WO) (HYPROMELLOSES - UNII:3NXW29V3WO)	HYPROMELLOSE, UNSPECIFIED	5 mg  in 1 mL
NAPHAZOLINE HYDROCHLORIDE (UNII: MZ1131787D) (NAPHAZOLINE - UNII:H231GF11BV)	NAPHAZOLINE HYDROCHLORIDE	0.3 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)
SODIUM CHLORIDE (UNII: 451W47IQ8X)
HYDROCHLORIC ACID (UNII: QTT17582CB)
SODIUM HYDROXIDE (UNII: 55X04QC32I)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 68788-6973-1	1 in 1 CARTON	06/07/2017
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	09/02/2010

Labeler - Preferred Pharmaceuticals Inc. (791119022)

Registrant - Preferred Pharmaceuticals Inc. (791119022)

Establishment
Name	Address	ID/FEI	Business Operations
Preferred Pharmaceuticals Inc.		791119022	RELABEL(68788-6973)