Rohto Relief description, usages, side effects, indications, overdosage, supplying and lots more!

Menu
Search

Rohto Relief

Rohto-Mentholatum (Vietnam) Co. Ltd.

Drug Facts


FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

Active ingredient

Hypromellose 0.2%

Tetrahydrozoline HCl 0.05%

Zinc sulfate 0.25%

Purpose

Hypromellose - Lubricant

Tetrahydrozoline HCl - Redness reliever

Zinc sulfate - Astringent

Rohto Relief Uses

  • •temporarily relieves redness of the eye and discomfort due to
    • ∘minor eye irritations
    • ∘exposure to wind and sun
  • •temporarily relieves burning and irritation due to dryness of the eye

Warnings

For external use only

Ask a doctor before use if you have

narrow angle glaucoma

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
  • •overuse may cause more eye redness
  • •pupils may become enlarged temporarily
  • •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) up to 4 times daily
  • •tightly snap on cap to seal

Rohto Relief 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, sodium borate

Principal Display Panel

Rohto Relief

hypromellose, tetrahydrozoline HCl, zinc sulfate LIQUID

Product Information

Product Type Human otc drug label Item Code (Source) NDC:75977-8149
Route of Administration OPHTHALMIC DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
HYPROMELLOSES 2 mg
TETRAHYDROZOLINE HYDROCHLORIDE TETRAHYDROZOLINE 0.5 mg
ZINC SULFATE 2.5 mg

Inactive Ingredients

Ingredient Name Strength
benzalkonium chloride
BORIC ACID
chlorobutanol
EDETATE DISODIUM
MENTHOL
polysorbate 80
POTASSIUM ASPARTATE
water
SODIUM BORATE

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 13 in 1 BOTTLE
2 NDC:75977-8149-1 1 in 1 CARTON

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
part part349 2013-06-01


PLEASE, BE CAREFUL!
Be sure to consult your doctor before taking any medication!
Copyright © 2014. drugs-library.com. All rights reserved. Information on drugs-library.com is provided for educational purposes only and is not to be used for medical advice, diagnosis or treatment.
Support info@drugs-library.com.