LEADER EYE DROPS REDNESS RELIEF- glycerin, naphazoline hydrochloride solution/ drops 
Cardinal Health

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Leader Eye Drops Redness Relief (PLD)

Active ingredients

Glycerin 0.25%

Naphazoline hydrochloride 0.012%

Purposes

Glycerin...Lubricant

Naphazoline hydrochloride...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 or 2 drops in the affected eye(s) up to 4 times daily

children under 6 years of age:ask a doctor

Other information

Inactive ingredients

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

Questions or comments?

Call  1-888-527-4276

carton

Twin size

LEADER EYE DROPS REDNESS RELIEF 
glycerin, naphazoline hydrochloride solution/ drops
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:70000-0010
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)  
BORIC ACID (UNII: R57ZHV85D4)  
EDETATE DISODIUM (UNII: 7FLD91C86K)  
WATER (UNII: 059QF0KO0R)  
SODIUM BORATE (UNII: 91MBZ8H3QO)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:70000-0010-11 in 1 CARTON04/30/2019
115 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product
2NDC:70000-0010-22 in 1 CARTON04/30/2019
215 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM01804/30/2019
Labeler - Cardinal Health (063997360)
Registrant - KC Pharmaceuticals, Inc. (174450460)
Establishment
NameAddressID/FEIBusiness Operations
KC Pharmaceuticals, Inc.174450460manufacture(70000-0010) , pack(70000-0010) , label(70000-0010)

Revised: 12/2023
Document Id: 0d37bf18-e4e8-6459-e063-6294a90af2ff
Set id: aee4bbe2-4f11-4c54-be8b-df48b3ba4f3a
Version: 4
Effective Time: 20231223
 
Cardinal Health