FDA.reportPublic FDA data

Equate Support Advanced Lubricant Drops MultiDose

Manufacturer
Wal-Mart Stores, Inc. | Altaire Pharmaceuticals, Inc.
Effective date
2018-04-18
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-02 00:55:18

Label at a glance#

ProductEquate Support Advanced Lubricant Drops MultiDose
Active ingredientPOLYETHYLENE GLYCOL 400, PROPYLENE GLYCOL
Label structure10 sections

Indications and uses

Relieves dryness of the eye. For the temporary relief of burning, irritation and discomfort due to dryness of the eye or exposure to the wind and sun May be used as a protectant against further irritation.

Dosage and administration

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

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

Walmart

Equate

Support Advanced

Lubricant Gel Drops Multi-Dose

Preservative Free 7.5mL

NDC 49035-878-52

Drug Facts

Active ingredients

OTC - ACTIVE INGREDIENT SECTION

Polyethylene Glycol 400 0.4%

Propylene Glycol 0.3%

Purpose

OTC - PURPOSE SECTION

Lubricant

Lubricant

Uses

INDICATIONS & USAGE SECTION

  • Relieves dryness of the eye.
  • For the temporary relief of burning, irritation and discomfort due to dryness of the eye or exposure to the wind and sun
  • May be used as a protectant against further irritation.

Warnings

WARNINGS SECTION

  • For use in the eyes only.  Retain outer carton for full product drug facts.

Do not use

OTC - DO NOT USE SECTION

  • if this product changes color or becomes cloudy.
  • if you are sensitive to any ingredient in this product.

When using this product

OTC - WHEN USING SECTION

  • do not touch tip of container to any surface avoid contamination.
  • remove contact lenses
  • replace cap after each use.
  • do not deliver more than 6 consecutive drops.

Stop use and ask a doctor if  

OTC - STOP USE SECTION

  • you feel eye pain.
  • changes in vision occur.
  • redness or irritation of the eye(s) gets worse, persists or lasts more than 72 hours.

Keep this and all drugs out of the reach of children. 

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, get medical help or contact a Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

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

1. Twist Open 2. Squeeze

Other information

OTHER SAFETY INFORMATION

  • Store at room temperature 15°-30°C (59°-86°F).

Inactive ingredients

INACTIVE INGREDIENT SECTION

Aminomethylpropanol, boric acid, gellan gum, magnesium chloride hexahydrate, potassium chloride, purified water, sodium chloride, sorbitol. May contain hydrochloric acid and/or sodium hydroxide to adjust pH.

Questions and comments?

OTC - QUESTIONS SECTION

  • 1 (888) 287-1915

PRINCIPAL DISPLAY PANEL

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

NDC 49035-878-52
equate
Support Advanced
Lubricant
Gel Drops
Multi-Dose
Preservative Free
Sterile
0.25 FL OZ (7.5mL)

PRINCIPAL DISPLAY PANEL NDC 49035-878-52 equate Support Advanced Lubricant Gel Drops Multi-Dose Preservative Free Sterile 0.25 FL OZ (7.5mL)PRINCIPAL DISPLAY PANEL NDC 49035-878-52 equate Support Advanced Lubricant Gel Drops Multi-Dose Preservative Free Sterile 0.25 FL OZ (7.5mL)

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
49035-878-522020-01-31C16284748780-19d75b9cf-cdfa-f424-e053-dadaa90a57ceEquate Support Advanced Lubricant Gel Drops MultiDose

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
49035-878EQUATE SUPPORT ADVANCED LUBRICANT DROPS MULTIDOSE (POLYETHYLENE GLYCOL 400, PROPYLENE GLYCOL) SOLUTION/ DROPS [WAL-MART STORES, INC.]2Legacy NDC20180601_306de2bf-4d5b-4421-8049-fdcfe9fd10eb.zip

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 14 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
49035-87849035-878-52

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 12 matching rows.

Name, UNII, Kind table
NameUNIIKind
POLYETHYLENE GLYCOL 400B697894SGQACTIB
PROPYLENE GLYCOL6DC9Q167V3ACTIB
AMINOMETHYLPROPANOLLU49E6626QIACT
BORIC ACIDR57ZHV85D4IACT
GELLAN GUM (LOW ACYL)7593U09I4DIACT
MAGNESIUM CHLORIDE02F3473H9OIACT
POTASSIUM CHLORIDE660YQ98I10IACT
WATER059QF0KO0RIACT
SODIUM CHLORIDE451W47IQ8XIACT
SORBITOL506T60A25RIACT
HYDROCHLORIC ACIDQTT17582CBIACT
SODIUM HYDROXIDE55X04QC32IIACT

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
b96792af-b672-4629-93f8-0575106501fe306de2bf-4d5b-4421-8049-fdcfe9fd10eb2018-04-18WarningsExact identifier
spl id: b96792af-b672-4629-93f8-0575106501fe
spl set id: 306de2bf-4d5b-4421-8049-fdcfe9fd10eb

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.