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Sunmark Redness Relief

Medically reviewed on Nov 7, 2016

Dosage form: liquid
Ingredients: GLYCERIN 0.2g in 100mL, NAPHAZOLINE HYDROCHLORIDE 0.012g in 100mL
Labeler: McKesson Corporation
NDC Code: 49348-894

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

Drug Facts

Active Ingredients

Glycerin 0.2%

Naphazoline hydrochloride 0.012%

Purpose

Lubricant and redness reliver

Uses
  • relieves redness of the eye due to minor eye irritations
  • for use as a protectant against further irritation or to relieve dryness of the eye
  • temporarily relieves burning and irritation due to dryness of the eye

Warnings

For external use only

Do not use this product if
  • solution changes color or become cloudy

Ask a doctor before use

if you have narrow angle glaucoma

when using this product
  • do not touch tip of container to any surface to avoid contamination
  • replace cap after using
  • overuse may cause more redness of the eye
  • pupils may become enlarged temporarily

Stop use and ask a doctor if
  • you feel eye pain
  • changes in vision occur
  • redness or irritation of the eye lasts
  • condition worsens
  • symptoms last for more than 72 hours

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 4 times daily

Other information
  • Tamper Evident. Do not use this product if imprinted neckband is missing or broken.
  • store at room temperature
  • remove contact lenses before using

Inactive ingredients

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

SUNMARK REDNESS RELIEF 
glycerin, naphazoline hydrochloride liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:49348-894
Route of AdministrationOPHTHALMICDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
GLYCERIN (GLYCERIN) GLYCERIN0.2 g  in 100 mL
NAPHAZOLINE HYDROCHLORIDE (NAPHAZOLINE) NAPHAZOLINE HYDROCHLORIDE0.012 g  in 100 mL
Inactive Ingredients
Ingredient NameStrength
BENZALKONIUM CHLORIDE 
BORIC ACID 
EDETATE DISODIUM 
WATER 
SODIUM BORATE 
Packaging
#Item CodePackage Description
1NDC:49348-894-291 BOTTLE, PLASTIC in 1 CARTON
115 mL in 1 BOTTLE, PLASTIC
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart34910/01/2009
Labeler - McKesson Corporation (177667227)
Registrant - KC Pharmaceuticals, Inc. (174450460)
Establishment
NameAddressID/FEIOperations
KC Pharmaceuticals, Inc.174450460manufacture(49348-894), pack(49348-894), label(49348-894)

 
McKesson Corporation

Further information

Always consult your healthcare provider to ensure the information displayed on this page applies to your personal circumstances.

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