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Rohto Hydra by The Mentholatum Company

Medically reviewed on July 31, 2017

Dosage form: liquid
Ingredients: HYDROXYETHYL CELLULOSE (2000 MPA.S AT 1%) 6mg in 1mL
Labeler: The Mentholatum Company
NDC Code: 10742-8148

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

Hydroxyethyl cellulose 0.6%

Purpose

Hydroxyethyl cellulose - Lubricant

Uses
temporarily relieves discomfort due to minor irritations of the eye or exposure to wind or 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
put 1 or 2 drops in the affected eye(s) as needed

Other information

store at 20-25 °C (68-77°F)
tightly snap on cap to seal

Inactive ingredients

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

Questions?

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

Principal Display Panel
ROHTO HYDRA 
hydroxyethyl cellulose liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:10742-8148
Route of AdministrationOPHTHALMICDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
HYDROXYETHYL CELLULOSE (2000 MPA.S AT 1%) (HYDROXYETHYL CELLULOSE (2000 MPA.S AT 1%)) HYDROXYETHYL CELLULOSE (2000 MPA.S AT 1%)6 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
BENZALKONIUM CHLORIDE 
BORIC ACID 
EDETATE DISODIUM 
MENTHOL, UNSPECIFIED FORM 
POLYSORBATE 80 
POTASSIUM CHLORIDE 
WATER 
SODIUM BORATE 
SODIUM CHLORIDE 
Packaging
#Item CodePackage Description
1NDC:10742-8148-11 BOTTLE, DROPPER in 1 CARTON
113 mL in 1 BOTTLE, DROPPER
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart34901/03/201110/31/2018
Labeler - The Mentholatum Company (002105757)

 
The Mentholatum Company

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Further information

Always consult your healthcare provider to ensure the information displayed on this page applies to your personal circumstances.

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