FDA.reportPublic FDA data

Drug Facts - Rohto Dual Light Relief

Manufacturer
The Mentholatum Company | Rohto Pharmaceutical Co., Ltd.
Effective date
2026-06-19
Label type
HUMAN OTC DRUG LABEL
Version
4
Source
monthly-update
Hydrated at
2026-07-17 21:34:48

Label at a glance#

ProductRohto Dual Light Relief
Active ingredientPOVIDONE, HYPROMELLOSE, UNSPECIFIED
Label structure8 sections

Indications and uses

for the temporary relief of discomfort due to minor irritations of the eye or to exposure to wind or sun protects against further irritation or to relieve dryness of the eye

Dosage and administration

put 1 or 2 drops in the affected eye(s) as needed tightly snap on cap to seal Other information do not store above 25 O C (77 O F)

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Hypromellose 0.3%

Povidone 0.5%

Purpose

OTC - PURPOSE SECTION

Hypromellose – Lubricant

Povidone - Lubricant

Uses

INDICATIONS & USAGE SECTION

  • for the temporary relief of discomfort due to minor irritations of the eye or to exposure to wind or sun
  • protects against further irritation or to relieve dryness of the eye

Warnings

WARNINGS SECTION

For external use only

When using this product

OTC - WHEN USING SECTION

  • 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

OTC - STOP USE SECTION

  • 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.

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

  • put 1 or 2 drops in the affected eye(s) as needed
  • tightly snap on cap to seal

Other information

  • do not store above 25 OC (77 OF)

Inactive ingredients

INACTIVE INGREDIENT SECTION

alginic acid, anhydrous citric acid, boric acid, camphor, chlorobutanol, edetate disodium, menthol, polysorbate 80, purified water, sodium borate, sodium citrate, taurine, zinc sulfate

Questions?

OTC - QUESTIONS SECTION

1-877-636-2677 MON-FRI 9AM-5PM (EST)

Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Dual Light ReliefDual Light Relief

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
QR code linkQR Codewww.rohtoreviews.com/Dual Light Relief.jpg

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
f47a510b-6679-4664-b2d6-47b5c4afe7ccProduct name420260217
e2db08c6-133f-4f4f-afb4-e90a2418d6f6Product name120230320
0306390c-dd77-4363-afe0-63c58088b2a1Product name120220120
503ea967-4b9c-48cf-9e87-c7975295849dProduct name220220120
ce6d5c06-3ae0-18a6-d5b3-8cd3cc0f8906Product name720210625
f52be47f-7aa7-46c0-b1fa-50c18dd50206Product name120201029
11ed6f83-cdd2-4637-8379-b1a1d3ae3cdeProduct name120181101
86c45a79-b9f0-4476-a27c-6e10db098497Product name120180125
d5e51f11-ad28-caa4-4b49-4143974782adProduct name120150831

Products#

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

DailyMed product names page 1 of 1 · 17 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
10742-845910742-8459-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 15 matching rows.

Name, UNII, Kind table
NameUNIIKind
EDETATE DISODIUM7FLD91C86KIACT
BORIC ACIDR57ZHV85D4IACT
LEVOMENTHOLBZ1R15MTK7IACT
POVIDONEFZ989GH94EACTIB
CHLOROBUTANOLHM4YQM8WRCIACT
TRISODIUM CITRATE DIHYDRATEB22547B95KIACT
ZINC SULFATE HEPTAHYDRATEN57JI2K7WPIACT
ALGINIC ACID8C3Z4148WZIACT
ANHYDROUS CITRIC ACIDXF417D3PSLIACT
HYPROMELLOSE, UNSPECIFIED3NXW29V3WOACTIB
POLYSORBATE 806OZP39ZG8HIACT
SODIUM BORATE91MBZ8H3QOIACT
TAURINE1EQV5MLY3DIACT
WATER059QF0KO0RIACT
CAMPHOR (SYNTHETIC)5TJD82A1ETIACT

Source Document#

Source XML

Older Hydrated Versions#

Version, Effective date, Source table
VersionEffective dateSourceHydrated
32024-12-19full-release2026-06-01 00:45:18

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
Rohto Dual Light ReliefHYPROMELLOSE, POVIDONEThe Mentholatum Company1b597f83-d7f1-cf93-e063-6394a90a99f72026-06-19WarningsExact identifier
ndc (package): 10742-8459-1
ndc (product): 10742-8459
ndc11 (package): 10742845901
spl id: 54a078be-963e-d967-e063-6294a90a800a
spl set id: 1b597f83-d7f1-cf93-e063-6394a90a99f7

Reported adverse events (FAERS/openFDA)#

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