ROHTO JOLT- hypromellose liquid 
The Mentholatum Company

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

----------

Drug Facts

Active ingredient

Hypromellose 0.35%

Purpose

Hypromellose - Lubricant

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

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
  • remove contact lenses before using

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 lasts more than 72 hours

Keep out of reach of children.

If swallowed, get medical help or contact a Poison Control Center right away.

Directions

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

Other Information

  • do not store above 25°C (77°F)

Inactive ingredients

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

Questions or comments?

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

Package/Label Principal Display Panel

Rohto Jolt Drug Facts
ROHTO JOLT 
hypromellose liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:10742-8194
Route of AdministrationOPHTHALMIC
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
HYPROMELLOSE 2906 (4000 MPA.S) (UNII: 5EYA69XGAT) (HYPROMELLOSE 2906 (4000 MPA.S) - UNII:5EYA69XGAT) HYPROMELLOSE 2906 (4000 MPA.S)3.5 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7)  
BORIC ACID (UNII: R57ZHV85D4)  
CHLOROBUTANOL (UNII: HM4YQM8WRC)  
EDETATE DISODIUM (UNII: 7FLD91C86K)  
MENTHOL, UNSPECIFIED FORM (UNII: L7T10EIP3A)  
POLYSORBATE 80 (UNII: 6OZP39ZG8H)  
POTASSIUM ASPARTATE (UNII: OC4598NZEQ)  
WATER (UNII: 059QF0KO0R)  
PYRIDOXINE HYDROCHLORIDE (UNII: 68Y4CF58BV)  
SODIUM BORATE (UNII: 91MBZ8H3QO)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:10742-8194-11 in 1 CARTON10/01/2017
113 mL in 1 BOTTLE, WITH APPLICATOR; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart34910/01/201712/31/2022
Labeler - The Mentholatum Company (002105757)

Revised: 2/2023
Document Id: f4c1ca97-64c8-69d3-e053-2995a90a3ccc
Set id: 0dc29577-6b66-428b-a46b-546973654841
Version: 3
Effective Time: 20230215
 
The Mentholatum Company