CAREONE MAXIMUM REDNESS RELIEF EYE DROPS- glycerin, naphazoline hci solution/ drops 
Retail Business Services, LLC

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CareOne Maximum Redness Relief Eye Drops (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 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.

Other information

Inactive ingredients

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

Questions or comments?

Call 1-888-527-4276

CareOne Maximum Redness Relief Eye Drops 15mL

CareOne Maximum Redness Relief Eye Drops 15mL

CAREONE MAXIMUM REDNESS RELIEF EYE DROPS 
glycerin, naphazoline hci solution/ drops
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:72476-012
Route of AdministrationOPHTHALMIC
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
GLYCERIN (UNII: PDC6A3C0OX) (GLYCERIN - UNII:PDC6A3C0OX) GLYCERIN0.5 g  in 100 mL
NAPHAZOLINE HYDROCHLORIDE (UNII: MZ1131787D) (NAPHAZOLINE - UNII:H231GF11BV) NAPHAZOLINE HYDROCHLORIDE0.03 g  in 100 mL
Inactive Ingredients
Ingredient NameStrength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7)  
BORIC ACID (UNII: R57ZHV85D4)  
SODIUM BORATE (UNII: 91MBZ8H3QO)  
EDETATE DISODIUM (UNII: 7FLD91C86K)  
WATER (UNII: 059QF0KO0R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:72476-012-011 in 1 BOX01/12/2020
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 DrugM01801/12/2020
Labeler - Retail Business Services, LLC (967989935)
Registrant - KC Pharmaceuticals, Inc. (174450460)
Establishment
NameAddressID/FEIBusiness Operations
KC Pharmaceuticals, Inc.174450460manufacture(72476-012) , pack(72476-012) , label(72476-012)

Revised: 12/2023
Document Id: 0d37dad1-219b-7c25-e063-6394a90a7eb7
Set id: 9ab96aed-21d3-11b6-e053-2995a90a7225
Version: 3
Effective Time: 20231223
 
Retail Business Services, LLC