Rohto Dual Light Relief

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: Rohto Dual Light Relief
Generic name: HYPROMELLOSE, POVIDONE
Manufacturer: The Mentholatum Company
Product type: HUMAN OTC DRUG
SPL set ID: 1b597f83-d7f1-cf93-e063-6394a90a99f7
SPL ID: 54a078be-963e-d967-e063-6294a90a800a
Version: 4
Effective date: 2026-06-19
Source export date: 2026-09-28
Source partition: 11
Source file: https://download.open.fda.gov/drug/label/drug-label-0011-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-09-28/aa96b5a2be6b394393acd0090f6948bdf99e0e8e00666f81608929c8fa83db77/drug-label-0011-of-0014.json.zip
Source manifest SHA-256: cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run: 20260929T050834Z
Imported at: 2026-09-29 06:18:17

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 · 12 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		M018	openfda.application_number
brand name		Rohto Dual Light Relief	openfda.brand_name
generic name		HYPROMELLOSE, POVIDONE	openfda.generic_name
manufacturer name		The Mentholatum Company	openfda.manufacturer_name
ndc	package	10742-8459-1	openfda.package_ndc
ndc	product	10742-8459	openfda.product_ndc
ndc11	package	10742845901	derived:openfda.package_ndc
rxcui		2604775	openfda.rxcui
spl id		54a078be-963e-d967-e063-6294a90a800a	id
spl set id		1b597f83-d7f1-cf93-e063-6394a90a99f7	set_id
unii		3NXW29V3WO	openfda.unii
unii		FZ989GH94E	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 For external use only When using this product do not touch tip of container to any surface to avoid contamination replace cap after each use do not use if solution changes color or becomes cloudy Stop use and ask a doctor if you feel eye pain changes in vision occur redness or irritation of the eyes lasts condition worsens or persists for more than 72 hours Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Reported adverse events (FAERS/openFDA)#

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