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Good Neighbor Pharmacy Eye Drop

Medically reviewed on November 13, 2017

Dosage form: solution/ drops
Ingredients: TETRAHYDROZOLINE HYDROCHLORIDE .05g in 100mL
Labeler: AmerisourceBergen Drug Corporation
NDC Code: 24385-075

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.

Good Neighbor Pharmacy Eye Drops

Drug Facts

Active Ingredient

Tetrahydrozoline HCl 0.05%

Purpose

Redness reliever

Uses

relieves redness of the eye due to minor eye irritations

Warnings

For external use only

Ask a doctor

before use if you havenarrow angle glaucoma

When using this product

  • pupils may become enlarged temporarily
  • to avoid contamination, do not touch tip of container to any surface. Replace cap after using.
  • if solution changes color or becomes cloudy, do not use
  • overuse may produce increased redness of the eye
  • remove contact lens before using

Stop use and ask a doctor if
  • eye pain
  • changes in vision
  • continued redness or irritation of the eye, or if the condition worsens or persists for 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

Instill 1 or 2 drops in the affected eye(s) up to four times daily.

Other information

Store at 15 °-30°C (59°-86°F)

Inactive ingredients

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

Good Neighbor Pharmacy Eye Drops

GOOD NEIGHBOR PHARMACY EYE DROP 
tetrahydrozoline hcl 0.05% solution/ drops
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:24385-075
Route of AdministrationINTRAOCULARDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
TETRAHYDROZOLINE HYDROCHLORIDE (TETRAHYDROZOLINE) TETRAHYDROZOLINE HYDROCHLORIDE.05 g  in 100 mL
Inactive Ingredients
Ingredient NameStrength
BENZALKONIUM CHLORIDE 
BORIC ACID 
EDETATE DISODIUM 
WATER 
SODIUM BORATE 
SODIUM CHLORIDE 
Packaging
#Item CodePackage Description
1NDC:24385-075-0515 mL in 1 BOTTLE, DROPPER
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart34901/29/2001
Labeler - AmerisourceBergen Drug Corporation (007914906)
Establishment
NameAddressID/FEIOperations
KC Pharmaceuticals, Inc.174450460manufacture(24385-075), label(24385-075)

 
AmerisourceBergen Drug Corporation

Disclaimer: Every effort has been made to ensure that the information provided here is accurate, up-to-date and complete, but no guarantee is made to that effect. Drug information contained herein may be time sensitive. This information has been compiled for use by healthcare practitioners and consumers in the United States. The absence of a warning for a given drug or combination thereof in no way should be construed to indicate that the drug or combination is safe, effective or appropriate for any given patient. If you have questions about the substances you are taking, check with your doctor, nurse or pharmacist.

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