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Signature Care Eye Drops Redness and Dry Eye Relief

Dosage form: liquid
Ingredients: GLYCERIN 0.25g in 100mL, NAPHAZOLINE HYDROCHLORIDE 0.012g in 100mL
Labeler: Better Living Brands LLC
NDC code: 21130-703

Medically reviewed by Drugs.com. Last updated on Jan 17, 2024.

Drug Facts

Active ingredients

Glycerin 0.25%

Naphazoline hydrochloride 0.012%

Purposes

Glycerin  Lubricant

Naphazoline hydrochloride   Redness reliever

Uses
  • for the relief of redness of the eye due to minor eye irritations
  • for the temporary relief of burining and irritation due to dryness of the eye 
  • for use as a protectant against further irritation or dryness of the eye

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
  • 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 (1-800-222-1222) right away.

Directions

Instill 1 or 2 drops in the affected eye(s) up to 4 times daily

Other information
  • store at room temperature
  • remove contact lenses before using

Inactive ingredients

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

SIGNATURE CARE EYE DROPS REDNESS AND DRY EYE RELIEF 
glycerin, naphazoline hydrochloride liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:21130-703
Route of AdministrationOPHTHALMICDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
GLYCERIN (GLYCERIN) GLYCERIN0.25 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:21130-703-011 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 finalpart34910/05/2018
Labeler - Better Living Brands LLC (009137209)
Registrant - KC Pharmaceuticals, Inc. (174450460)
Establishment
NameAddressID/FEIOperations
KC Pharmaceuticals, Inc.174450460manufacture(21130-703), pack(21130-703), label(21130-703)

Revised: 01/2019
Document Id: ee7b725a-e5d8-4d1f-b46e-04bfba718700
Set id: 901f3bbe-e1bb-4e44-879c-711e59813a7f
Version: 2
Effective Time: 20190127
 
Better Living Brands LLC

Further information

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

Medical Disclaimer