EYE DROPS- carboxymethylcellulose sodium liquid

EYE DROPS by

Drug Labeling and Warnings

EYE DROPS by is a Otc medication manufactured, distributed, or labeled by Foshan Sugar Max Cosmetics CO.,Ltd. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

SPL UNCLASSIFIED SECTION

EYE DROPS

ACTIVE INGREDIENT

Carboxymethylcellulose sodium 0.25%

PURPOSE

Eye lubricant

INDICATIONS & USAGE

Uses For the temporary relief of burning, irritation, anddiscomfort due to dryness of the eye or exposure towind or sun.
May be used as a protectant against further irritation.

WARNINGS

For external use only.
To avoid contamination, do not touch tip of container toany surface. Replace cap after using.
lf solution changes color or becomes cloudy, do not use.

STOP USE

Stop use and ask a doctor if you experience eye pain,changes in vision, continued redness or irritation of theeye, or if the condition worsens or persists for more than72 hours.

KEEP OUT OF REACH OF CHILDREN

Keep out of reach of children. lf swallowed, get medicalhelp or contact a Poison Control Center right away.

DOSAGE & ADMINISTRATION

Directions Instilllor 2 drops in the affected eye(s) asneeded

STORAGE AND HANDLING

Use only if tape seals on top and bottom flaps areintact.
Use before expiration date marked on container.
Discard 90 days after opening.

INACTIVE INGREDIENT

calciumchloride
Dequest
magnesium chloride
potassium chloride
purified water
sodium bicarbonate
sodium chloride
sodium perborate
sodium phosphate

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

EYE DROPS 
carboxymethylcellulose sodium liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 84938-001
Route of Administration	OPHTHALMIC

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
CARBOXYMETHYLCELLULOSE SODIUM, UNSPECIFIED (UNII: K679OBS311) (CARBOXYMETHYLCELLULOSE - UNII:05JZI7B19X)	CARBOXYMETHYLCELLULOSE SODIUM, UNSPECIFIED	0.25 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
CALCIUM CHLORIDE ANHYDROUS (UNII: OFM21057LP)
SODIUM CHLORIDE (UNII: 451W47IQ8X)
POTASSIUM CHLORIDE (UNII: 660YQ98I10)
WATER (UNII: 059QF0KO0R)
SODIUM PERBORATE (UNII: Y52BK1W96C)
SODIUM BICARBONATE (UNII: 8MDF5V39QO)
SODIUM PHOSPHATE (UNII: SE337SVY37)
AMINOTRIS(METHYLENEPHOSPHONIC ACID) (UNII: 1Y702GD0FG)
MAGNESIUM CHLORIDE (UNII: 02F3473H9O)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 84938-001-01	2 in 1 BOX	11/14/2024
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	11/14/2024

Labeler - Foshan Sugar Max Cosmetics CO.,Ltd (700689935)

Establishment
Name	Address	ID/FEI	Business Operations
Foshan Sugar Max Cosmetics CO.,Ltd		700689935	manufacture(84938-001)