Carboxymethylcellulose Sodium Ophthalmic Gel 1%

Carboxymethylcellulose Sodium Ophthalmic Gel 1%
SPL v6
SPL
SPL Set ID b469f1c4-bd94-6f50-e053-2995a90a452f
Route
OPHTHALMIC
Published
Effective Date 2020-11-18
Document Type 34390-5 HUMAN OTC DRUG LABEL

Drug Facts

Composition & Product

Active Ingredients
Carboxymethylcellulose (10 mg)
Inactive Ingredients
Boric Acid Calcium Chloride Magnesium Chloride Potassium Chloride Water Sodium Borate Sodium Chloride

Identifiers & Packaging

Marketing Status
OTC MONOGRAPH DRUG Active Since 2020-11-18

Description

Drug Facts

Purpose

Eye lubricant


Medication Information

Purpose

Eye lubricant

Description

Drug Facts

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.
Section 42229-5

Drug Facts

Section 50565-1

Keep this and all drugs out of the reach of children. If swallowed, get medical help or contact a Poison Control Center right away (1-800-222-1222).

Section 50566-9

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.

Section 51945-4

Warnings
  • For use in the eyes 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

Shake well before use.

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

Active Ingredient

Carboxymethylcellulose sodium 1%

Other Information
  • Do Not Use if imprinted seal on cap is torn, broken or missing.
  • Discard 90 days after opening.
  • Store at room temperature 15°-30°C (59°-86°F).
  • Retain outer carton for full product drug information.
Inactive Ingredients

Boric acid, calcium chloride, magnesium chloride, potassium chloride, purified water, sodium borate, sodium chloride. Stabilized Oxychloro Complex 2.5%. May contain hydrochloric acid and/or sodium hydroxide to adjust pH.

Questions Or Comments?

1-855-361-3993

Distributed by:

AvKARE

Pulaski, TN 38478

Rev. 09/2020 AV 09/2020


Structured Label Content

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.
Section 42229-5 (42229-5)

Drug Facts

Section 50565-1 (50565-1)

Keep this and all drugs out of the reach of children. If swallowed, get medical help or contact a Poison Control Center right away (1-800-222-1222).

Section 50566-9 (50566-9)

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.

Section 51945-4 (51945-4)

Purpose

Eye lubricant

Warnings
  • For use in the eyes 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

Shake well before use.

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

Active Ingredient (Active ingredient)

Carboxymethylcellulose sodium 1%

Other Information (Other information)
  • Do Not Use if imprinted seal on cap is torn, broken or missing.
  • Discard 90 days after opening.
  • Store at room temperature 15°-30°C (59°-86°F).
  • Retain outer carton for full product drug information.
Inactive Ingredients (Inactive ingredients)

Boric acid, calcium chloride, magnesium chloride, potassium chloride, purified water, sodium borate, sodium chloride. Stabilized Oxychloro Complex 2.5%. May contain hydrochloric acid and/or sodium hydroxide to adjust pH.

Questions Or Comments? (Questions or comments?)

1-855-361-3993

Distributed by:

AvKARE

Pulaski, TN 38478

Rev. 09/2020 AV 09/2020


Advanced Ingredient Data


Raw Label Data

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