EQUATE REDNESS AND DRY EYE RELIEF EYE DROPS- glycerin, naphazoline hcl solution/ drops 
Wal-Mart Stores, Inc.

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Equate Redness and Dry Eye Relief Eye Drops 15mL (PLD)

Active ingredients

Glycerin 0.25%

Naphazoline HCl 0.012%

Purposes

Lubricant

Redness reliever

Uses

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 doctor 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 4 times daily

Other information

store at room temperature

Inactive ingredients

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

Questions or comments?

1-888-287-1915

Equate Redness and Dry Eye Relief Eye Drops 15mL

Equate Redness and Dry Eye Relief Eye Drops 15mL

EQUATE REDNESS AND DRY EYE RELIEF EYE DROPS 
glycerin, naphazoline hcl solution/ drops
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:79903-012
Route of AdministrationOPHTHALMIC
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
GLYCERIN (UNII: PDC6A3C0OX) (GLYCERIN - UNII:PDC6A3C0OX) GLYCERIN0.25 g  in 100 mL
NAPHAZOLINE HYDROCHLORIDE (UNII: MZ1131787D) (NAPHAZOLINE - UNII:H231GF11BV) NAPHAZOLINE HYDROCHLORIDE0.012 g  in 100 mL
Inactive Ingredients
Ingredient NameStrength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7)  
EDETATE DISODIUM (UNII: 7FLD91C86K)  
WATER (UNII: 059QF0KO0R)  
SODIUM BORATE (UNII: 91MBZ8H3QO)  
BORIC ACID (UNII: R57ZHV85D4)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:79903-012-011 in 1 BOX12/12/2020
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 DrugM01812/12/2020
Labeler - Wal-Mart Stores, Inc. (051957769)
Registrant - KC Pharmaceuticals, Inc. (174450460)
Establishment
NameAddressID/FEIBusiness Operations
KC Pharmaceuticals, Inc.174450460manufacture(79903-012) , pack(79903-012) , label(79903-012)

Revised: 12/2023
Document Id: 0d383700-e254-881f-e063-6294a90a347c
Set id: ae228018-9238-2cbd-e053-2995a90a8d99
Version: 5
Effective Time: 20231223
 
Wal-Mart Stores, Inc.