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

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Rohto Relief

The Mentholatum Company
The Mentholatum Company

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

Inactive ingredients

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

Package/Label Principal Display Panel

Principal Display Panel

Rohto Relief

hypromellose, tetrahydrozoline HCl, zinc sulfate LIQUID

Product Information

Product Type Human otc drug label Item Code (Source) NDC:10742-8149
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:10742-8149-1 1 in 1 CARTON

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
part part349 2011-12-01


PLEASE, BE CAREFUL!
Be sure to consult your doctor before taking any medication!
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