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 Type	HUMAN OTC DRUG	Item Code (Source)	NDC:21130-703
Route of Administration	OPHTHALMIC	DEA Schedule

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
GLYCERIN (GLYCERIN)	GLYCERIN	0.25 g in 100 mL
NAPHAZOLINE HYDROCHLORIDE (NAPHAZOLINE)	NAPHAZOLINE HYDROCHLORIDE	0.012 g in 100 mL

Inactive Ingredients
Ingredient Name	Strength
BENZALKONIUM CHLORIDE
BORIC ACID
EDETATE DISODIUM
WATER
SODIUM BORATE

Packaging
#	Item Code	Package Description
1	NDC:21130-703-01	1 BOTTLE, PLASTIC in 1 CARTON
1		15 mL in 1 BOTTLE, PLASTIC

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part349	10/05/2018

Labeler - Better Living Brands LLC (009137209)

Registrant - KC Pharmaceuticals, Inc. (174450460)

Establishment
Name	Address	ID/FEI	Operations
KC Pharmaceuticals, Inc.		174450460	manufacture(21130-703), pack(21130-703), label(21130-703)

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