Rugby Artificial Tears

Manufacturer
NuCare Pharmaceuticals,Inc.
Effective date
2020-09-30
Label type
HUMAN OTC DRUG LABEL
Version
4
Source
legacy-cache
Hydrated at
2026-08-01 23:11:04

Label at a glance#

ProductRugby Artificial Tears
Active ingredientPOLYVINYL ALCOHOL
Label structure11 sections

Storage and handling

Other information - store at 15° - 25°C (59° - 77°F) - keep tightly closed

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active ingredient                                                               Purpose

Polyvinyl Alcohol 1.4%...................................................Lubricant

OTC - PURPOSE SECTION

Uses

- relieves dryness of the eye

- prevents further irritation

WARNINGS SECTION

Do not use

- if solution changes color or becomes cloudy

- with contact lenses

OTC - WHEN USING SECTION

- do not touch tip of container to any surface to avoid contamination

- replace cap after each use

OTC - ASK DOCTOR SECTION

Stop use and ask a doctor

- if you experience eye pain, changes in vision, continued redness or irritation of the eye

- condition worsens or persists for more than 72 hours

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children

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

INDICATIONS & USAGE SECTION

Directions

- instill 1 to 2 drops in the affected eye(s) as needed

STORAGE AND HANDLING SECTION

Other information

- store at 15° - 25°C (59° - 77°F)

- keep tightly closed

INACTIVE INGREDIENT SECTION

Inactive ingredients

benzalkonium chloride, dibasic sodium phosphate hydrate, edetate disodium hydrate, monobasic sodium phosphate dihydrate, purified water, sodium chloride

DOSAGE & ADMINISTRATION SECTION

Distributed by:

Rugby Laboratories

31778 Enterprise Drive

Livonia, MI 48150

www.rugbylaboratories.com

Rugby Laboratories

Made in Korea

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

PDPPDP

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
68071-4149-52020-09-23C16284748780-1ab0b4bfd-9d17-d255-e053-dadaa90ae5915d7edc99-68fd-09a1-e053-2a91aa0a15fe

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
0536-1084-94ML - Milliliter0536-1084a9936793-2edf-4e26-9482-451d3d53b8f512015-12-02

Products#

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

DailyMed product names page 1 of 1 · 8 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
68071-414968071-4149-5
0536-1084

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 7 matching rows.

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
1a3a64e0-490c-da00-e063-6294a90a9ea45d7edc99-68fd-09a1-e053-2a91aa0a15fe2024-06-06WarningsExact identifier
spl set id: 5d7edc99-68fd-09a1-e053-2a91aa0a15fe

Reported adverse events (FAERS/openFDA)#

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