MEIJER MAXIMUM REDNESS RELIEF AND LUBRICANT- glycerin, naphazoline hci solution/ drops 
Meijer Distribution, Inc.

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Meijer Maximum Redness Relief & Lubricant15mL (PLD)

Active ingredients

Glycerin 0.5%

Naphazoline HCI 0.03%

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 contract 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

Inactive ingredients

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

Questions or comments?

Call 1-888-527-4276

Meijer Maximum Redness Relief and Lubricant 15mL

Meijer Maximum Redness Relief and Lubricant 15mL

MEIJER MAXIMUM REDNESS RELIEF AND LUBRICANT 
glycerin, naphazoline hci solution/ drops
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:41250-715
Route of AdministrationOPHTHALMIC
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
NAPHAZOLINE HYDROCHLORIDE (UNII: MZ1131787D) (NAPHAZOLINE - UNII:H231GF11BV) NAPHAZOLINE HYDROCHLORIDE0.03 g  in 100 mL
GLYCERIN (UNII: PDC6A3C0OX) (GLYCERIN - UNII:PDC6A3C0OX) GLYCERIN0.5 g  in 100 mL
Inactive Ingredients
Ingredient NameStrength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7)  
SODIUM BORATE (UNII: 91MBZ8H3QO)  
BORIC ACID (UNII: R57ZHV85D4)  
EDETATE DISODIUM (UNII: 7FLD91C86K)  
WATER (UNII: 059QF0KO0R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:41250-715-011 in 1 BOX03/11/2020
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 DrugM01803/11/2020
Labeler - Meijer Distribution, Inc. (006959555)
Registrant - KC Pharmaceuticals, Inc. (174450460)
Establishment
NameAddressID/FEIBusiness Operations
KC Pharmaceuticals, Inc.174450460manufacture(41250-715) , pack(41250-715) , label(41250-715)

Revised: 12/2023
Document Id: 0d2273c9-17e2-0f0b-e063-6294a90a76da
Set id: 9feb1818-c79b-23bf-e053-2995a90a1084
Version: 3
Effective Time: 20231222
 
Meijer Distribution, Inc.