UP AND UP LUBRICANT REFRESHING- carboxymethylcellulose sodium solution/ drops

Up and Up Lubricant Refreshing by

Drug Labeling and Warnings

Up and Up Lubricant Refreshing by is a Otc medication manufactured, distributed, or labeled by Target Corporation. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Active ingredient Purpose

Carboxymethylcellulose sodium 0.5%..........................Eye lubricant

PURPOSE

Uses

• for the temporary relief of burning, irritation, and discomfort due to dryness of the eye or exposure to wind or sun
• may be used as a protectant against further irritation

WARNINGS

Warnings

For external use only

WHEN USING

When using this product

• do not touch tip of container to any surface to avoid contamination
• do not reuse
• once opened, discard
• do not use if this solution changes color or becomes cloudy
• remove contact lenses before using

STOP USE

Stop use and ask a doctor if

• you feel eye pain
• changes in vision occur
• continued redness or irritation of the eye lasts
• condition worsens or lasts more than 72 hours

PREGNANCY OR BREAST FEEDING

If pregnant or breast-feeding, ask a health professional before use.

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.

INDICATIONS & USAGE

Directions

• to open, twist and pull tab to remove
• instill 1 or 2 drops in the affected eye(s) as needed
• children under 6 years of age: ask a doctor

STORAGE AND HANDLING

Other information

• store between 15-30°C (59-86°F)
• protect from light

INACTIVE INGREDIENT

Inactive ingredients calcium chloride, hydrochloric acid, magnesium chloride, potassium chloride, purified water, sodium chloride, sodium hydroxide, sodium lactate

DOSAGE & ADMINISTRATION

Distributed by:

Target Corporation

Minneapolis, MN 55403

Made in South Korea

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

UP AND UP LUBRICANT REFRESHING 
carboxymethylcellulose sodium solution/ drops

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 11673-636
Route of Administration	OPHTHALMIC

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
CARBOXYMETHYLCELLULOSE SODIUM (UNII: K679OBS311) (CARBOXYMETHYLCELLULOSE - UNII:05JZI7B19X)	CARBOXYMETHYLCELLULOSE SODIUM	5 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
CALCIUM CHLORIDE (UNII: M4I0D6VV5M)
HYDROCHLORIC ACID (UNII: QTT17582CB)
MAGNESIUM CHLORIDE (UNII: 02F3473H9O)
POTASSIUM CHLORIDE (UNII: 660YQ98I10)
SODIUM HYDROXIDE (UNII: 55X04QC32I)
SODIUM LACTATE (UNII: TU7HW0W0QT)
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 11673-636-70	70 in 1 CARTON	04/19/2018
1		0.4 mL in 1 VIAL; 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	04/19/2018

Labeler - Target Corporation (006961700)