KROGER MOISTURIZING LUBRICANT- carboxymethylcellulose sodium solution/ drops

Kroger Moisturizing Lubricant by

Drug Labeling and Warnings

Kroger Moisturizing Lubricant by is a Otc medication manufactured, distributed, or labeled by The Kroger Co.. 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
• replace cap after each use
• 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

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

STORAGE AND HANDLING

Other information

• store between 15-30°C (59-86°F)

INACTIVE INGREDIENT

Inactive ingredients

benzalkonium chloride, boric acid, calcium chloride, hydrochloric acid, magensium chloride, potassium chloride, purified water, sodium borate, sodium chloride, sodium hydroxide

DOSAGE & ADMINISTRATION

Distributed by:

The Kroger Co.

Cincinnati, Ohio 45202

Made in South Korea

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

KROGER MOISTURIZING LUBRICANT 
carboxymethylcellulose sodium solution/ drops

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 30142-412
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
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7)
BORIC ACID (UNII: R57ZHV85D4)
CALCIUM CHLORIDE (UNII: M4I0D6VV5M)
HYDROCHLORIC ACID (UNII: QTT17582CB)
MAGNESIUM CHLORIDE (UNII: 02F3473H9O)
POTASSIUM CHLORIDE (UNII: 660YQ98I10)
WATER (UNII: 059QF0KO0R)
SODIUM BORATE (UNII: 91MBZ8H3QO)
SODIUM CHLORIDE (UNII: 451W47IQ8X)
SODIUM HYDROXIDE (UNII: 55X04QC32I)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 30142-412-15	1 in 1 CARTON	04/20/2018
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	04/20/2018

Labeler - The Kroger Co. (006999528)