UP AND UP DRY EYE RELIEF LUBRICANT EYE DROPS- carboxymethylcellulose sodium solution/ drops

Up and Up Dry Eye Relief Lubricant Eye Drops by

Drug Labeling and Warnings

Up and Up Dry Eye Relief Lubricant Eye Drops by is a Otc medication manufactured, distributed, or labeled by Hanlim. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Carboxymethylcellulose Sodium 0.5%

PURPOSE

Purpose.......Lubricant

KEEP OUT OF REACH OF CHILDREN

If swallowed, get medical help or contact a Poison Control Center immediately (1-800-222-1222) right away.

DOSAGE & ADMINISTRATION

Instill 1 or 2 drops in the affected eye(s) as needed

INDICATIONS & USAGE

• For the temporary relief of burning, irritation, and discomfort due to dryness of the eye or from irritation from wind or sun.
• May be used to protect against further irritation.

WARNINGS

WARNINGS

• Warnings - For external use only.

DO NOT USE

• Do not use - if solution changes color or becomes cloudy
• If you are sensitive or allergic to any ingredient in this product

WHEN USING

• To avoid contamination, do not touch tip of container to any surface.
• Replace cap after using.

STOP USE
Stop use and ask a doctor if

• you experience eye pain
• changes in vision occur
• redness or irritation of the eye(s) gets worse or lasts more than 72 hours

INACTIVE INGREDIENT

Inactive ingredients: benzalkonium chloride, boric acid, calcium chloride hydrate, hydrochloric acid, magnesium chloride, potassium chloride, sodium borate, sodium chloride, sodium hydroxide, water

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

UP AND UP DRY EYE RELIEF LUBRICANT EYE DROPS 
carboxymethylcellulose sodium solution/ drops

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 11716-0771
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
SODIUM BORATE (UNII: 91MBZ8H3QO)
WATER (UNII: 059QF0KO0R)
SODIUM CHLORIDE (UNII: 451W47IQ8X)
CALCIUM CHLORIDE (UNII: M4I0D6VV5M)
HYDROCHLORIC ACID (UNII: QTT17582CB)
MAGNESIUM CHLORIDE (UNII: 02F3473H9O)
SODIUM HYDROXIDE (UNII: 55X04QC32I)
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7)
BORIC ACID (UNII: R57ZHV85D4)
POTASSIUM CHLORIDE (UNII: 660YQ98I10)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 11716-0771-1	2 in 1 BOX	10/31/2025
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 Drug	M018	10/31/2025

Labeler - Hanlim (687986034)