OTC Medication Information: Equate Redness Reliever

EQUATE REDNESS RELIEVER- tetrahydrozoline hydrochloride solution/ drops
WALMART INC.

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

Tetrahydrozoline Hydrochloride 0.05%

Purpose

Redness reliever

Uses

  • relieves redness of the eye due to minor eye irritations

Warnings

For external use only

Do not use

  • if solution changes color or becomes cloudy

Ask a doctor before use if you have

  • narrow angle glaucoma

When using this product

  • to avoid contamination, do not touch tip of container to any surface
  • replace cap after using
  • overuse may produce increased redness of the eye
  • pupils may become enlarged temporarily

Stop use and ask a d octor if

  • you experience eye pain
  • you experience changes in vision
  • you experience continued redness or irritation of the eye
  • the 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 (1-800-222-1222) right away.

Directions

  • instill 1 to 2 drops in the affected eye(s) up to four times daily

Other i nformation

  • store at room temperature
  • remove contact lenses before using

Inactive ingredients

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

Questions?

1-888-287-1915

Principal Display Panel

Equate
Redness Reliever
Tetrahydrozoline HCI

Eye Drops

0.5 FL OZ (15 mL)

Principal Display Panel 
Equate™
Redness Reliever
Tetrahydrozoline HCI
Eye Drops
0.5 FL OZ (15 mL)
(click image for full-size original)

Principal Display Panel

Equate
Redness Reliever
Tetrahydrozoline HCI
Eye Drops

1 FL OZ (30 mL)

Principal Display Panel 
Equate™
Redness Reliever
Tetrahydrozoline HCI
Eye Drops
1 FL OZ (30 mL)
(click image for full-size original)
EQUATE REDNESS RELIEVER
tetrahydrozoline hydrochloride solution/ drops
Product Information
Product Type HUMAN OTC DRUG Item Code (Source) NDC:79903-010
Route of Administration OPHTHALMIC DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
TETRAHYDROZOLINE HYDROCHLORIDE (TETRAHYDROZOLINE) TETRAHYDROZOLINE HYDROCHLORIDE 0.5 mg in 1 mL
Inactive Ingredients
Ingredient Name Strength
BENZALKONIUM CHLORIDE
BORIC ACID
EDETATE DISODIUM
WATER
SODIUM BORATE
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:79903-010-15 1 BOTTLE in 1 CARTON contains a BOTTLE
1 15 mL in 1 BOTTLE This package is contained within the CARTON (79903-010-15)
2 NDC:79903-010-30 1 BOTTLE in 1 CARTON contains a BOTTLE
2 30 mL in 1 BOTTLE This package is contained within the CARTON (79903-010-30)
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
OTC MONOGRAPH FINAL part349 04/26/2013
Labeler — WALMART INC. (051957769)

Revised: 09/2020 WALMART INC.

Our database comes directly from the FDA’s central repository of drug labels and package inserts under the Structured Product Labeling standard. OTCLabels.com provides the full over the counter products subset of the FDA’s repository. Medication information provided here is not intended as a substitute for direct consultation with a qualified health professional.

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Our database comes directly from the FDA's central repository of drug labels and package inserts under the Structured Product Labeling standard. OTCLabels.com provides the full over the counter products subset of the FDA's repository. Medication information provided here is not intended as a substitute for direct consultation with a qualified health professional.

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