Rugby Lubricating Drops

openFDA label record#

This page contains supplementary openFDA label data. For the canonical label presentation, use the corresponding DailyMed Structured Product Label.

Verified complete openFDA source JSON (canonical bytes are SHA-256 checked before publication)

Brand name: Rugby Lubricating Drops
Generic name: POLYVINYL ALCOHOL
Manufacturer: A-S Medication Solutions
Product type: HUMAN OTC DRUG
SPL set ID: f2e26f85-4081-425b-9c81-ac2a079a5743
SPL ID: 19ea574c-7ae8-4577-9189-c095bbc131e2
Version: 4
Effective date: 2023-11-10
Source export date: 2026-10-12
Source partition: 3
Source file: https://download.open.fda.gov/drug/label/drug-label-0003-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-10-12/f40eac55ff4c5d55c3d8bbc5766ea7e21e4196960cfb4703b96a406b491c0cd5/drug-label-0003-of-0014.json.zip
Source manifest SHA-256: 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run: 20261013T011858Z
Imported at: 2026-10-13 01:30:59

Harmonized routes table
Harmonized routes
OPHTHALMIC

Harmonized identifier links#

Every typed identifier imported from the complete openFDA harmonization object is paginated here; values are not reduced to a first match.

Harmonized identifiers page 1 of 1 · 11 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		M018	openfda.application_number
brand name		Rugby Lubricating Drops	openfda.brand_name
generic name		POLYVINYL ALCOHOL	openfda.generic_name
manufacturer name		A-S Medication Solutions	openfda.manufacturer_name
ndc	package	50090-5996-0	openfda.package_ndc
ndc	product	50090-5996	openfda.product_ndc
ndc11	package	50090599600	derived:openfda.package_ndc
rxcui		142004	openfda.rxcui
spl id		19ea574c-7ae8-4577-9189-c095bbc131e2	id
spl set id		f2e26f85-4081-425b-9c81-ac2a079a5743	set_id
unii		532B59J990	openfda.unii

Warnings cross-check#

openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.

Warnings sections page 1 of 1 · 1 matching rows.

warnings

Warnings Do not use if solution changes color or becomes cloudy When using this product do not touch tip of container to any surface to avoid contamination remove contact lens before using. replace cap after using. keep container tightly closed 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

Reported adverse events (FAERS/openFDA)#

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