FDA.reportPublic FDA data

Drug Facts - Rohto Dry-Aid

Manufacturer
The Mentholatum Company | Rohto Pharmaceutical Co. Ltd.
Effective date
2026-08-18
Label type
HUMAN OTC DRUG LABEL
Version
11
Source
daily-update
Hydrated at
2026-08-21 02:01:15

Label at a glance#

ProductRohto Dry-Aid
Active ingredientPOVIDONE, UNSPECIFIED, PROPYLENE GLYCOL
Label structure8 sections

Indications and uses

temporarily relieves burning and irritation due to dryness of the eye 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 freeze

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Povidone 0.68%

Propylene glycol 0.3%

Purpose

OTC - PURPOSE SECTION

Povidone – Lubricant

Propylene glycol - Lubricant

Uses

INDICATIONS & USAGE SECTION

  • temporarily relieves burning and irritation due to dryness of the eye
  • 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 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) as needed
  • tightly snap on cap to seal

Other information

  • do not freeze

Inactive ingredients

INACTIVE INGREDIENT SECTION

boric acid, calcium chloride, edetate disodium, magnesium sulfate, menthol, PEG-10 castor oil, poloxamer, polyaminopropyl biguanide, polyoxyl stearate, purified water, sesame oil, sodium borate

Questions?

OTC - QUESTIONS SECTION

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

Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Carton
Carton

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
95250459-30e4-45c1-b08a-993044f49109Product name220250805
30b0ac6e-02aa-0e5c-0d8b-cffdf3a282b2Product name520250304
362d7abb-94e6-4c60-9a58-266894157713Product name120231023
9badc7be-250a-44ab-aa36-926af3f02679Product name120210527
444b3e50-f226-46ef-bfca-2e7035d140cdProduct name120190611
7cda52fc-125f-421c-8fea-bc1974370c49Product name220180703
26acd337-b838-40ac-bcbc-05c3b81c8712Product name120170323
d5e51f11-ad28-caa4-4b49-4143974782adProduct name120150831
0ca1d589-929b-4b33-bc5b-1d84abdafa6aProduct name120150324
fc363c46-397b-4476-ac0f-70e43e8e4592Product name120150324
87711080-88eb-65c5-b2dd-bf99e700a372Product name120140508
ec2149b3-5c6d-5344-f757-c86411073075Product name120140508

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
10742-8162-12023-02-07C16284748780-1f386c64a-0139-0266-e053-dadaa90a7c1aDrug Facts - Rohto Dry-Aid
10742-8162-12023-02-07C16284748780-1f386c64a-0139-0266-e053-dadaa90a7c1aDrug Facts - Rohto Dry-Aid
10742-8162-22023-02-07C16284748780-1f386c64a-0139-0266-e053-dadaa90a7c1aDrug Facts - Rohto Dry-Aid
10742-8162-22023-02-07C16284748780-1f386c64a-0139-0266-e053-dadaa90a7c1aDrug Facts - Rohto Dry-Aid
10742-8162-12023-01-30C16284748780-1f386c64a-0139-0266-e053-dadaa90a7c1aDrug Facts - Rohto Dry-Aid
10742-8162-12023-01-30C16284748780-1f386c64a-0139-0266-e053-dadaa90a7c1aDrug Facts - Rohto Dry-Aid
10742-8162-22023-01-30C16284748780-1f386c64a-0139-0266-e053-dadaa90a7c1aDrug Facts - Rohto Dry-Aid
10742-8162-22023-01-30C16284748780-1f386c64a-0139-0266-e053-dadaa90a7c1aDrug Facts - Rohto Dry-Aid

Products#

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

DailyMed product names page 1 of 1 · 16 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
10742-816210742-8162-1, 10742-8162-2

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 14 matching rows.

Name, UNII, Kind table
NameUNIIKind
POVIDONE, UNSPECIFIEDFZ989GH94EACTIB
PROPYLENE GLYCOL6DC9Q167V3ACTIB
BORIC ACIDR57ZHV85D4IACT
CALCIUM CHLORIDEM4I0D6VV5MIACT
EDETATE DISODIUM7FLD91C86KIACT
MAGNESIUM SULFATE ANHYDROUSML30MJ2U7IIACT
RACEMENTHOLYS08XHA860IACT
POLYOXYL 35 CASTOR OIL6D4M1DAL6OIACT
PEG/PPG-105/5 COPOLYMER52901V8XARIACT
POLIHEXANIDE HYDROCHLORIDE4XI6112496IACT
POLYOXYL 40 STEARATE13A4J4NH9IIACT
WATER059QF0KO0RIACT
SESAME OILQX10HYY4QVIACT
SODIUM BORATE91MBZ8H3QOIACT

Source Document#

Source XML

Older Hydrated Versions#

Version, Effective date, Source table
VersionEffective dateSourceHydrated
102024-12-17full-release2026-06-01 00:44:15

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 Dry-AidPOVIDONE, PROPYLENE GLYCOLThe Mentholatum Company8ea5c6c9-48f4-406a-a2cb-9280c546d87d2026-08-18WarningsExact identifier
ndc (package): 10742-8162-2
ndc (package): 10742-8162-1
ndc (product): 10742-8162
ndc11 (package): 10742816201
ndc11 (package): 10742816202
spl id: 59588453-9990-ef56-e063-6394a90a7e4a
spl set id: 8ea5c6c9-48f4-406a-a2cb-9280c546d87d

Reported adverse events (FAERS/openFDA)#

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