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Drug Facts

Manufacturer
The Mentholatum Company | Rohto-Mentholatum (Vietnam) Co. Ltd.
Effective date
2026-08-20
Label type
HUMAN OTC DRUG LABEL
Version
6
Source
daily-update
Hydrated at
2026-08-22 01:01:29

Label at a glance#

ProductRohto All-In-One
Active ingredientHYPROMELLOSE, UNSPECIFIED, TETRAHYDROZOLINE HYDROCHLORIDE, ZINC SULFATE, UNSPECIFIED FORM
Label structure8 sections

Indications and uses

temporarily relieves redness of the eye and discomfort due to minor eyes irritations exposure to wind or sun temporarily relieves burning and irritation due to dryness of the eye

Dosage and administration

put 1 or 2 drops in the affected eye(s) up to 4 times daily tightly snap on cap to seal Other information store at 20-25°C (68-77°F)

Label contents#

Full prescribing information#

Active ingredients

OTC - ACTIVE INGREDIENT SECTION

Hypromellose 0.2%

Tetrahydrozoline HCl 0.05%

Zinc sulfate 0.25%

Purpose

OTC - PURPOSE SECTION

Hypromellose - Lubricant

Tetrahydrozoline HCl - Redness reliever

Zinc sulfate - Astringent

Uses

INDICATIONS & USAGE SECTION

  • temporarily relieves redness of the eye and discomfort due to
    • minor eyes irritations
    • exposure to wind or sun
  • temporarily relieves burning and irritation due to dryness of the eye

Warnings

WARNINGS SECTION

For external use only

Ask a doctor before use if you have narrow angle glaucoma

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
  • overuse may cause more eye redness
  • pupils may become enlarged temporarily

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 lasts 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) up to 4 times daily
  • tightly snap on cap to seal

Other information

  • store at 20-25°C (68-77°F)

Inactive ingredients

INACTIVE INGREDIENT SECTION

boric acid, edetate disodium, menthol, polysorbate 80, purified water, sodium borate

Questions?

OTC - QUESTIONS SECTION

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

Package Label/Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Image 1Image 1

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
BarcodeEAN-130310742010862GTIN-13: 0310742010862
EAN-13: 0310742010862
GTIN-12: 310742010862
UPC-A: 310742010862
GTIN storage (14 digits): 00310742010862		CA517004-Rohto All-In-One.jpg
QR code linkQR Codewww.rohtoreviews.com/CA517004-Rohto All-In-One.jpg

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
f47a510b-6679-4664-b2d6-47b5c4afe7ccProduct name420260217
030ce964-9b2d-45aa-b5d3-f78ce03ef61cProduct name220250515
0306390c-dd77-4363-afe0-63c58088b2a1Product name120220120
503ea967-4b9c-48cf-9e87-c7975295849dProduct name220220120
190f2a5b-bbc8-65c7-fcb0-97891307b917Product name120140508
27945931-b6e2-158e-d615-4ef21e2af974Product name120140508

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
10742-8146-12023-02-08C16284748780-1f386c649-adf7-0266-e053-dadaa90a7c1aDrug Facts
10742-8146-12023-02-08C16284748780-1f386c649-adf7-0266-e053-dadaa90a7c1aDrug Facts
10742-8146-12023-02-08C16284748780-1f386c649-adf7-0266-e053-dadaa90a7c1aDrug Facts
10742-8146-12023-01-30C16284748780-1f386c649-adf7-0266-e053-dadaa90a7c1aDrug Facts
10742-8146-12023-01-30C16284748780-1f386c649-adf7-0266-e053-dadaa90a7c1aDrug Facts
10742-8146-12023-01-30C16284748780-1f386c649-adf7-0266-e053-dadaa90a7c1aDrug Facts

Products#

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

DailyMed product names page 1 of 1 · 13 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
10742-814610742-8146-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 9 matching rows.

Name, UNII, Kind table
NameUNIIKind
HYPROMELLOSE, UNSPECIFIED3NXW29V3WOACTIB
TETRAHYDROZOLINE HYDROCHLORIDE0YZT43HS7DACTIB
ZINC SULFATE, UNSPECIFIED FORM89DS0H96TBACTIB
MENTHOL, UNSPECIFIED FORML7T10EIP3AIACT
POLYSORBATE 806OZP39ZG8HIACT
WATER059QF0KO0RIACT
SODIUM BORATE91MBZ8H3QOIACT
EDETATE DISODIUM7FLD91C86KIACT
BORIC ACIDR57ZHV85D4IACT

Source Document#

Source XML

Older Hydrated Versions#

Version, Effective date, Source table
VersionEffective dateSourceHydrated
52026-06-03daily-update2026-06-06 05:10:19
32024-12-17full-release2026-06-01 00:44:11

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 All-In-OneHYPROMELLOSE, TETRAHYDROZOLINE HYDROCHLORIDE, ZINC SULFATEThe Mentholatum Company43e690e4-b381-46e3-838c-33aef5bdadde2026-08-20WarningsExact identifier
ndc (package): 10742-8146-1
ndc (product): 10742-8146
ndc11 (package): 10742814601
spl id: 597621d4-3b06-4f1d-e063-6294a90a7073
spl set id: 43e690e4-b381-46e3-838c-33aef5bdadde

Reported adverse events (FAERS/openFDA)#

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