REFRESH DIGITAL- carboxymethylcellulose sodium, glycerin, polysorbate 80 solution/ drops

Refresh Digital by

Drug Labeling and Warnings

Refresh Digital by is a Otc medication manufactured, distributed, or labeled by Allergan, Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug Facts      

Active ingredients

Carboxymethylcellulose sodium 0.5%

Glycerin 1%

Polysorbate 80 0.5%

Purpose

Eye lubricant

Eye lubricant

Eye 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.
  
• To avoid contamination, do not touch tip of container to any surface. Replace cap after using.
  
• If solution changes color, do not use.

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 right away.

Directions

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

Other information

• Use only if tape seals on top and bottom flaps are intact.
  
• Use before expiration date marked on container.
  
• Discard 90 days after opening.
  
• Store at 59°-77°F (15°-25°C).
  
• RETAIN THIS CARTON FOR FUTURE REFERENCE.

Inactive ingredients

Boric acid; carbomer copolymer type A; castor oil; erythritol; levocarnitine; purified water; PURITE® (stabilized oxychloro complex); and sodium hydroxide (to adjust pH).

Questions or comments?

  1.800.678.1605

refreshbrand.com

v1.0DFL6952

PRINCIPAL DISPLAY PANEL

NDC: 0023-6952-10

Refresh®
 Digital
Lubricant Eye Drops
For Eye Dryness
with
HydroCell™
Fast-acting Relief
That Soothes Your Eyes
0.33 fl oz (10 mL) Sterile

INGREDIENTS AND APPEARANCE

REFRESH DIGITAL 
carboxymethylcellulose sodium, glycerin, polysorbate 80 solution/ drops

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 0023-6952
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
GLYCERIN (UNII: PDC6A3C0OX) (GLYCERIN - UNII:PDC6A3C0OX)	GLYCERIN	10 mg  in 1 mL
POLYSORBATE 80 (UNII: 6OZP39ZG8H) (POLYSORBATE 80 - UNII:6OZP39ZG8H)	POLYSORBATE 80	5 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
BORIC ACID (UNII: R57ZHV85D4)
CARBOMER COPOLYMER TYPE A (UNII: 71DD5V995L)
CASTOR OIL (UNII: D5340Y2I9G)
ERYTHRITOL (UNII: RA96B954X6)
LEVOCARNITINE (UNII: 0G389FZZ9M)
WATER (UNII: 059QF0KO0R)
SODIUM HYDROXIDE (UNII: 55X04QC32I)
SODIUM CHLORITE (UNII: G538EBV4VF)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0023-6952-10	1 in 1 CARTON	08/01/2020
1		10 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product
2	NDC: 0023-6952-02	1 in 1 CARTON	08/01/2020
2		2 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	08/01/2020

Labeler - Allergan, Inc. (144796497)