ROHTO DUAL LIGHT RELIEF- hypromellose, povidone liquid 
The Mentholatum Company

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Drug Facts - Rohto Dual Light Relief

Active ingredient

Hypromellose 0.3%

Povidone 0.5%

Purpose

Hypromellose – Lubricant

Povidone - Lubricant

Uses

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

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 persists for more than 72 hours

Keep out of reach of children.

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

Directions

Other information

Inactive ingredients

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

Questions?

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

Principal Display Panel

Principal Display Panel

Dual Light Relief

ROHTO  DUAL LIGHT RELIEF
hypromellose, povidone liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:10742-8459
Route of AdministrationOPHTHALMIC
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
POVIDONE (UNII: FZ989GH94E) (POVIDONE - UNII:FZ989GH94E) POVIDONE5 mg  in 1 mL
HYPROMELLOSE, UNSPECIFIED (UNII: 3NXW29V3WO) (HYPROMELLOSE, UNSPECIFIED - UNII:3NXW29V3WO) HYPROMELLOSE, UNSPECIFIED3 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
LEVOMENTHOL (UNII: BZ1R15MTK7)  
EDETATE DISODIUM (UNII: 7FLD91C86K)  
BORIC ACID (UNII: R57ZHV85D4)  
CHLOROBUTANOL (UNII: HM4YQM8WRC)  
TRISODIUM CITRATE DIHYDRATE (UNII: B22547B95K)  
ZINC SULFATE HEPTAHYDRATE (UNII: N57JI2K7WP)  
ALGINIC ACID (UNII: 8C3Z4148WZ)  
ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)  
POLYSORBATE 80 (UNII: 6OZP39ZG8H)  
SODIUM BORATE (UNII: 91MBZ8H3QO)  
TAURINE (UNII: 1EQV5MLY3D)  
WATER (UNII: 059QF0KO0R)  
CAMPHOR (SYNTHETIC) (UNII: 5TJD82A1ET)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:10742-8459-11 in 1 CARTON05/30/2024
118 mL in 1 BOTTLE, DISPENSING; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM01805/30/2024
Labeler - The Mentholatum Company (002105757)
Registrant - The Mentholatum Company (002105757)
Establishment
NameAddressID/FEIBusiness Operations
The Mentholatum Company002105757label(10742-8459)
Establishment
NameAddressID/FEIBusiness Operations
Rohto Pharmaceutical Co., Ltd.696604024manufacture(10742-8459)

Revised: 12/2024
Document Id: 29aaa211-07f2-71e1-e063-6294a90a1e43
Set id: 1b597f83-d7f1-cf93-e063-6394a90a99f7
Version: 3
Effective Time: 20241219
 
The Mentholatum Company