LEADER LUBRICANT EYE DROPS SOOTHING RELIEF- carboxymethylcellulose sodium solution/ drops

Leader Lubricant Eye Drops Soothing Relief by

Drug Labeling and Warnings

Leader Lubricant Eye Drops Soothing Relief by is a Otc medication manufactured, distributed, or labeled by LEADER/Cardinal Health 110, Inc., KC Pharmaceuticals, Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active ingredient

Carboxymethylcellulose sodium 0.5%

Purpose

Lubricant

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

For external use only

Do not use

• if this product changes color or becomes cloudy
• if you are sensitive to any ingredient in this product

When using this product

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

Stop use and ask a doctor if you experience

• eye pain
• changes in vision
• continued redness or irritation of the eye, or if the 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 (1-800-222-1222) right away.

Directions

instill 1 to 2 drops in the affected eye(s) as needed

Other information

store at 15-25ºC (59-77ºF)

Inactive ingredients

benzalkonium chloride, boric acid, calcium chloride hydrate (dihydrate), **hydrochloric acid, magnesium chloride, potassium chloride, sodium borate, sodium chloride, **sodium hydroxide, water for injection

**May contain these ingredients to adjust pH.

Questions or comments?

Call 1-888-527-4276

Leader Lubricant Eye Drops Soothing Relief 15mL

Leader Lubricant Eye Drops Soothing Relief 15mL twin pk

INGREDIENTS AND APPEARANCE

LEADER LUBRICANT EYE DROPS SOOTHING RELIEF 
carboxymethylcellulose sodium solution/ drops

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 70000-0705
Route of Administration	OPHTHALMIC

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
CARBOXYMETHYLCELLULOSE SODIUM (UNII: K679OBS311) (CARBOXYMETHYLCELLULOSE - UNII:05JZI7B19X)	CARBOXYMETHYLCELLULOSE SODIUM	0.5 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
SODIUM HYDROXIDE (UNII: 55X04QC32I)
WATER (UNII: 059QF0KO0R)
BORIC ACID (UNII: R57ZHV85D4)
CALCIUM CHLORIDE MONOHYDRATE (UNII: LEV48803S9)
HYDROCHLORIC ACID (UNII: QTT17582CB)
POTASSIUM CHLORIDE (UNII: 660YQ98I10)
SODIUM BORATE (UNII: 91MBZ8H3QO)
SODIUM CHLORIDE (UNII: 451W47IQ8X)
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7)
MAGNESIUM CHLORIDE (UNII: 02F3473H9O)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 70000-0705-1	1 in 1 BOX	09/06/2024
1		15 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product
2	NDC: 70000-0705-2	2 in 1 BOX	09/06/2024
2		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	09/06/2024

Labeler - LEADER/Cardinal Health 110, Inc. (063997360)

Registrant - KC Pharmaceuticals, Inc. (174450460)