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T-RAOJO

Medically reviewed by Drugs.com. Last updated on Jul 7, 2021.

Dosage form: liquid
Ingredients: TETRAHYDROZOLINE HYDROCHLORIDE 0.5mg in 1mL
Labeler: Promex, LLC
NDC Code: 58988-0148

Drug Facts

Active Ingredient
  • Tetrahydrozoline HCl 0.5%

Purpose
  • Redness reliever

Use
  • for the relief of redness of the eye due to minor eye irritations

Warnings

Ask a doctor before use if you have narrow angle glaucoma

When using this product
  • pupils may become enlarged temporarily
  • overuse may cause more eye redness
  • remove contact lenses before using
  • do not use if this solution changes color or become cloudy
  • do not touch tip of container to any surface to avoid contamination
  • replace cap after each use

Stop use and ask a doctor if
  • you feel eye pain
  • changes in vision occur
  • redness or irritation of the eye lasts
  • condition worsens or lasts more than 72 hours

If pregnant or breast-feeding,

ask a health professional before use.

Keep out of reach of children.

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

Directions
  • Put 1 to 2 drops in the affected eye(s) up to 4 times daily
  • children under 6 years of age:  ask a doctor

Other information

  • store between 15° to 25°C (59°F to 77°F)


Inactive ingredients

benzalkonium chloride, boric acid, edetate disodium, hydrochloric acid, purified water, sodium borate, sodium chloride

package label

Redness relief

T-RAOJO 
tetrahydrozoline hydrochloride liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:58988-0148
Route of AdministrationOPHTHALMICDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
TETRAHYDROZOLINE HYDROCHLORIDE (TETRAHYDROZOLINE) TETRAHYDROZOLINE HYDROCHLORIDE0.5 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
BORIC ACID 
SODIUM BORATE 
EDETATE DISODIUM 
BENZALKONIUM CHLORIDE 
SODIUM CHLORIDE 
WATER 
HYDROCHLORIC ACID 
Packaging
#Item CodePackage Description
1NDC:58988-0148-51 BOTTLE (BOTTLE) in 1 BOX
115 mL in 1 BOTTLE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart34907/17/2014
Labeler - Promex, LLC (789974388)

Document Id: b776833e-2216-4e51-aee0-e80aa0a44ae5
Set id: 779d736d-0d1a-47a1-b5b0-f7fc7d44d383
Version: 1
Effective Time: 20140717
 
Promex, LLC

Further information

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

Medical Disclaimer