FDA.reportPublic FDA data

Rohto Jolt

Manufacturer
The Mentholatum Company
Effective date
2018-12-12
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-02 00:17:48

Label at a glance#

ProductRohto Jolt
Active ingredientHYPROMELLOSE 2906 (4000 MPA.S)
Label structure9 sections

Indications and uses

• temporarily relieves discomfort due to minor irritations of the eye or exposure to wind and sun • lubricates to prevent 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

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Hypromellose 0.35%

Purpose

OTC - PURPOSE SECTION

Hypromellose - Lubricant

Uses

INDICATIONS & USAGE SECTION

  • temporarily relieves discomfort due to minor irritations of the eye or exposure to wind and sun
  • lubricates to prevent 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
  • remove contact lenses before using

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

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

Other Information

OTHER SAFETY INFORMATION

  • do not store above 25°C (77°F)

Inactive ingredients

INACTIVE INGREDIENT SECTION

benzalkonium chloride, boric acid, chlorobutanol, edetate disodium, menthol, polysorbate 80, potassium aspartate, purified water, pyridoxine hydrochloride, sodium borate

Questions or comments?

OTC - QUESTIONS SECTION

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

Package/Label Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Rohto Jolt Drug Facts
Rohto Jolt Drug Facts

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
10742-8194-12023-03-23C16284748780-1f386c64a-4644-0266-e053-dadaa90a7c1aDrug Facts
10742-8194-12023-01-30C16284748780-1f386c64a-4644-0266-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
10742-819410742-8194-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 11 matching rows.

Name, UNII, Kind table
NameUNIIKind
HYPROMELLOSE 2906 (4000 MPA.S)5EYA69XGATACTIB
BENZALKONIUM CHLORIDEF5UM2KM3W7IACT
BORIC ACIDR57ZHV85D4IACT
CHLOROBUTANOLHM4YQM8WRCIACT
EDETATE DISODIUM7FLD91C86KIACT
MENTHOL, UNSPECIFIED FORML7T10EIP3AIACT
POLYSORBATE 806OZP39ZG8HIACT
POTASSIUM ASPARTATEOC4598NZEQIACT
WATER059QF0KO0RIACT
PYRIDOXINE HYDROCHLORIDE68Y4CF58BVIACT
SODIUM BORATE91MBZ8H3QOIACT

Source Document#

Source XML

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
4402b4e3-657f-f8c9-e063-6294a90a9d5b0dc29577-6b66-428b-a46b-5469736548412025-11-20WarningsExact identifier
spl set id: 0dc29577-6b66-428b-a46b-546973654841

Reported adverse events (FAERS/openFDA)#

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