DG LUBRICANT EYE DROPS- polyethylene glycol 400, propylene glycol solution

DG Lubricant Eye Drops by

Drug Labeling and Warnings

DG Lubricant Eye Drops by is a Otc medication manufactured, distributed, or labeled by Dolgencorp LLC, K.C. Pharmaceuticals, Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Active ingredients

Polyethylene glycol 400 0.4%

Propylene glycol 0.3%

PURPOSE

Active ingredients

Polyethylene glycol .....Lubricant

Propylene glycol.....Lubricant

INDICATIONS & USAGE

Uses

• for the temporary relief of burning and irritation due to dryness of the eye

WARNINGS

Warnngs

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

• do not touch the tip of container to any surface to avoid contamination
• replace cap after each use

Stop use and ask a doctor if

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

Keep out of reach of children

If swallowed, get medical help or contact a Poison Control Center right away

DOSAGE & ADMINISTRATION

Directions

• Instill 1 or 2 drops in the affected eye(s) as needed
• Children under 6 years of age: ask a doctor

OTHER SAFETY INFORMATION

Other information

• RETAIN THIS CARTON FOR FUTURE REFERENCE
• Store at room temperature

INACTIVE INGREDIENT

Inactive ingredients

Benzalkonium chloride as preservative, boric acid, calcium chloride, hypromellose, magnesium chloride, potassium chloride, purified water, sodium borate, sodium chloride, zinc chloride

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

DG LUBRICANT EYE DROPS 
polyethylene glycol 400, propylene glycol solution

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 55910-364
Route of Administration	OPHTHALMIC

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
PROPYLENE GLYCOL (UNII: 6DC9Q167V3) (PROPYLENE GLYCOL - UNII:6DC9Q167V3)	PROPYLENE GLYCOL	0.3 g  in 100 mL
POLYETHYLENE GLYCOL 400 (UNII: B697894SGQ) (POLYETHYLENE GLYCOL 400 - UNII:B697894SGQ)	POLYETHYLENE GLYCOL 400	0.4 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
CALCIUM CHLORIDE (UNII: M4I0D6VV5M)
HYPROMELLOSE, UNSPECIFIED (UNII: 3NXW29V3WO)
SODIUM BORATE (UNII: 91MBZ8H3QO)
BORIC ACID (UNII: R57ZHV85D4)
POTASSIUM CHLORIDE (UNII: 660YQ98I10)
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7)
ZINC CHLORIDE (UNII: 86Q357L16B)
MAGNESIUM CHLORIDE (UNII: 02F3473H9O)
WATER (UNII: 059QF0KO0R)
SODIUM CHLORIDE (UNII: 451W47IQ8X)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 55910-364-01	1 in 1 CARTON	01/27/2020
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	01/27/2020

Labeler - Dolgencorp LLC (068331990)

Registrant - K.C. Pharmaceuticals, Inc. (174450460)

Establishment
Name	Address	ID/FEI	Business Operations
K.C. Pharmaceuticals, Inc.		174450460	manufacture(55910-364) , pack(55910-364) , label(55910-364)