Equate Lubricant Eye Drops

Equate Lubricant Eye Drops
SPL v2
SPL
SPL Set ID 44494842-e38d-617c-e063-6294a90afaf8
Route
OPHTHALMIC
Published
Effective Date 2025-12-26
Document Type 34390-5 HUMAN OTC DRUG LABEL

Drug Facts

Composition & Product

Active Ingredients
Carboxymethylcellulose (0.5 mg)
Inactive Ingredients
Sodium Chloride Sodium Hydroxide Hydrochloric Acid Potassium Chloride Sodium Borate Calcium Chloride Monohydrate Benzalkonium Chloride Water Magnesium Chloride Boric Acid

Identifiers & Packaging

Marketing Status
OTC MONOGRAPH DRUG Active Since 2025-12-26

Description

Purpose: Lubricant


Medication Information

Warnings and Precautions

Warnings

For external use only

Do not use

■ If thisproduct changes color or becomes cloudy

■ if you are sensitive to any ingredient in this product

When using 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 to the

condition worsens or persists for more than 72 hours

Indications and Usage

Uses

■ for the temporary relief of burning, irritation, and discomfort due to dryness of the eye or exposure to wind or sun

■ maybe used as a protectant against further irritation

Dosage and Administration

Directions:

instill 1 to2 drops in the affected eye(s) as needed

Description

Purpose: Lubricant

Section 50565-1

Keep out of reach of children.

If swallowed, get medical help or contact a Poison Control Center(1-800-222-1222) right away.

Section 51727-6

Inactive ingredients

benzalkonium chloride,boric acid, calcium chloride hydrate (dihydrate), hydrochloric acid**, magnesium chloride, potassium chloride, sodium borate, sodium chloride, sodium hydroxide**, water for injection **may contain hydrochloric acid and sodium hydroxide to adjust pH

Section 51945-4

Section 55105-1

Purpose: Lubricant

Section 55106-9

Active ingredient

Carboxymethylcellulose sodium 0.5%.


Structured Label Content

Indications and Usage (34067-9)

Uses

■ for the temporary relief of burning, irritation, and discomfort due to dryness of the eye or exposure to wind or sun

■ maybe used as a protectant against further irritation

Dosage and Administration (34068-7)

Directions:

instill 1 to2 drops in the affected eye(s) as needed

Warnings and Precautions (34071-1)

Warnings

For external use only

Do not use

■ If thisproduct changes color or becomes cloudy

■ if you are sensitive to any ingredient in this product

When using 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 to the

condition worsens or persists for more than 72 hours

Section 50565-1 (50565-1)

Keep out of reach of children.

If swallowed, get medical help or contact a Poison Control Center(1-800-222-1222) right away.

Section 51727-6 (51727-6)

Inactive ingredients

benzalkonium chloride,boric acid, calcium chloride hydrate (dihydrate), hydrochloric acid**, magnesium chloride, potassium chloride, sodium borate, sodium chloride, sodium hydroxide**, water for injection **may contain hydrochloric acid and sodium hydroxide to adjust pH

Section 51945-4 (51945-4)

Section 55105-1 (55105-1)

Purpose: Lubricant

Section 55106-9 (55106-9)

Active ingredient

Carboxymethylcellulose sodium 0.5%.


Advanced Ingredient Data


Raw Label Data

All Sections (JSON)