WE FRESH LUBRICATING EYE DROPS- glycerin solution/ drops

Drug Labeling and Warnings

Drug Details [pdf]

SPL UNCLASSIFIED SECTION

Drug Facts

Active ingredient

Glycerin 0.25%

Purpose

Eye lubricant

Uses

 For the temporary relief of burning and irritation due to dryness of the eye

 For the temporary relief of discomfort due to minor irritations of the eye or to exposure to wind or sun

 For use as a protectant against further irritation or to relieve dryness of the eye.

Warnings

• For external use only

• Do not use if solution changes color or becomes cloudy.
• If tamper evident ring is broken or missing.

When usining this product

When usining 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, discontinue use and consult a doctor.

Keep out of reach of children.If swallowed, get medical help or contact a Poison Control Center right away.

Directions

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

Other Information

• Store at 15°-25°C (59°-77°F).

Inactive ingredients

Borate, boric acid, calcium chloride, l-carnitine, sodium chloride, sodium hyaluronate

PRINCIPAL DISPLAY PANEL - 10 ML Bottle Carton

INGREDIENTS AND APPEARANCE

WE FRESH  LUBRICATING EYE DROPS
glycerin solution/ drops

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 62144-0011
Route of Administration	OPHTHALMIC

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
GLYCERIN (UNII: PDC6A3C0OX) (GLYCERIN - UNII:PDC6A3C0OX)	GLYCERIN	2.5 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
SODIUM CHLORIDE (UNII: 451W47IQ8X)
WATER (UNII: 059QF0KO0R)
SODIUM BORATE (UNII: 91MBZ8H3QO)
BORIC ACID (UNII: R57ZHV85D4)
LEVOCARNITINE (UNII: 0G389FZZ9M)
CALCIUM CHLORIDE (UNII: M4I0D6VV5M)
SODIUM HYALURONATE (UNII: YSE9PPT4TH)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 62144-0011-0	1 in 1 CARTON	04/09/2026
1		10 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	04/08/2026

Labeler - Oculus Surgical, Inc. (015409582)