Drug Facts

Drug Facts

Drug Labeling and Warnings

Drug Details

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LUBRICANT AND REDNESS RELIEVER- naphazoline hydrochloride and polyethylene glycol 300 solution/ drops 
Target Corporation

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

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Drug Facts

Active Ingredients

Naphazoline Hydrochloride (0.012%)

Polyethylene Glycol 300 (0.2%)

Purpose

Redness reliever

Lubricant

Uses

• Relieves redness of the eye due to minor eye irritations.
• Temporary relief of burning and irritation due to dryness of the eye.
• Protects against further irritation.

Warnings

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
• serious side effects associated with use of the product may be reported to the phone number provided below

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?

Call 1-800-910-6874

DO NOT USE IF IMPRINTED

NECKBAND “PROTECTIVE SEAL”

WITH YELLOW IS NOT INTACT

245 09 0329 R00

ID074438

Distributed by

Target Corporation

Minneapolis, MN 55403

Made in U.S.A.

© 2014 Target Brands, Inc.

Shop Target.com

UPC – 4 92450 90329 9

9361700

JE55811

Package/Label Principal Display Panel

NDC: 11673-451-15

lubricant and

redness reliever

eye drops

for regular eye dryness

fast-acting formula

helps relieve redness due

to minor eye irritations

up&up®

STERILE

0.5 FL OZ (15 mL)

LUBRICANT AND REDNESS RELIEVER 
naphazoline hydrochloride and polyethylene glycol 300 solution/ drops

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 11673-451
Route of Administration	OPHTHALMIC

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
NAPHAZOLINE HYDROCHLORIDE (UNII: MZ1131787D) (NAPHAZOLINE - UNII:H231GF11BV)	NAPHAZOLINE HYDROCHLORIDE	0.1 mg  in 1 mL
POLYETHYLENE GLYCOL 300 (UNII: 5655G9Y8AQ) (POLYETHYLENE GLYCOL 300 - UNII:5655G9Y8AQ)	POLYETHYLENE GLYCOL 300	2 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: 11673-451-15	1 in 1 CARTON
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	09/13/2010

Labeler - Target Corporation (006961700)

Registrant - Bausch & Lomb Incorporated (196603781)

Establishment
Name	Address	ID/FEI	Business Operations
Bausch & Lomb Incorporated		114406598	MANUFACTURE(11673-451)

Establishment
Name	Address	ID/FEI	Business Operations
Bausch & Lomb Incorporated		079587625	MANUFACTURE(11673-451)

Revised: 10/2015

Document Id: f97034b0-a82a-4493-adab-b0765c50e202

Set id: 650281c7-4db8-4dc9-98f4-2976a7926f7d

Version: 3

Effective Time: 20151016

 

Target Corporation