GOOD NEIGHBOR PHARMACY EYE DROPS ORIGINAL FORMULA- tetrahydrozoline hcl 0.05% solution/ drops 
AmerisourceBergen Drug Corporation

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Good Neighbor Pharmacy Eye Drops Original (PLD)

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 have narrow 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 you experience

  • 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

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GOOD NEIGHBOR PHARMACY EYE DROPS ORIGINAL FORMULA 
tetrahydrozoline hcl 0.05% solution/ drops
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:24385-075
Route of AdministrationOPHTHALMIC
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
TETRAHYDROZOLINE HYDROCHLORIDE (UNII: 0YZT43HS7D) (TETRAHYDROZOLINE - UNII:S9U025Y077) TETRAHYDROZOLINE HYDROCHLORIDE0.05 g  in 100 mL
Inactive Ingredients
Ingredient NameStrength
BORIC ACID (UNII: R57ZHV85D4)  
EDETATE DISODIUM (UNII: 7FLD91C86K)  
WATER (UNII: 059QF0KO0R)  
SODIUM BORATE (UNII: 91MBZ8H3QO)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:24385-075-051 in 1 CARTON01/29/2001
115 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM01801/29/2001
Labeler - AmerisourceBergen Drug Corporation (007914906)
Registrant - K.C. Pharmaceuticals, Inc. (174450460)
Establishment
NameAddressID/FEIBusiness Operations
KC Pharmaceuticals, Inc.174450460manufacture(24385-075) , label(24385-075) , pack(24385-075)

Revised: 12/2023
Document Id: 0cfa2cc7-bb82-af55-e063-6394a90a28f0
Set id: 1e39e3a5-34fe-4e73-8f5c-219c4ef31bfb
Version: 5
Effective Time: 20231220
 
AmerisourceBergen Drug Corporation