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Biolle Gel Tears

Dosage form
SOLUTION/ DROPS
Labeler
SAGE Ethnographic Research, dba Biollé
Label updated
2016-04-13
Retrieved
2026-09-07
Active ingredients
Carboxymethylcellulose Sodium, Unspecified Form
View original label and images on DailyMed ↗
Label information

Drug Facts

Active ingredient

Carboxymethylcellulose sodium 1%

Purpose

Eye lubricant

Inactive Ingredients

Boric Acid, calcium chloride; magnesium chloride, potassium chloride; purified water, sodium borate; and sodium chloride. May contain sodium hydroxide and/or hydrochloric acid to adjust pH.

Uses
  • -For 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.
Label information

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.

Label information

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

Other Information
  • -Use before expiration date marked on container.
  • -Store at 59-86 F (15-30C).
  • -Retain this carton for future reference.
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 or becomes cloudy, do not use.
Directions

[Image in the official label — see DailyMed source]

To open, twist and pull tab to remove.

[Image in the official label — see DailyMed source]

Drop 1 to 2 drops in the affected eye as needed and discard the container.

Label information

Distributed by:
Biollé Inc.
PO Box 1386
New York, NY 10185

PRINCIPAL DISPLAY PANEL - 32 Vial Carton

Preservative-Free

Biollé
Gel Tears®

Rejuvenation in every drop

Severe dry eye relief

32 Single-use containers
0.02 fl oz (0.6mL) each sterile

[Image in the official label — see DailyMed source]

DailyMed Set ID: 9f70669f-37eb-4d6f-a8d4-a143835b0290 · Version 1
NDC: 69994-002