SIGNATURE CARE EYE DROPS HIGH PERFORMANCE- polyethylene glycol 400, propylene glycol solution/ drops 
Better Living Brands LLC

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Signature Care Eye Drops High Performance 15 mL (PLD)

Active ingredients

Polyethylene glycol 400  0.4%
Propylene glycol   0.3%

Purpose

Polyethylene glycol 400............. Lubricant
Propylene glycol............ Lubricant

Uses
• for the temporary relief of burning and irritation due to dryness of the eye

Warnings
For external use only

Do not use
• if this product changes color or becomes cloudy
• if you are sensitive to any ingredient in this product

When using this product
• do not touch the tip of container to any surface to avoid contamination
• replace cap after each use

Stop use and ask a doctor if
• you feel eye pain
• changes in vision occur
• redness or irritation of the eye(s) gets worse or lasts more than 72 hours

If pregnant or breast-feeding, ask a health professional before use.

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) as needed
• Children under 6 years of age: ask a doctor

Other information
store at 15°-30°C (59º-86ºF)

aminomethylpropanol, benzalkonium chloride as preservative, boric acid, hypromellose, potassium chloride, purified water, sodium chloride, sorbitol

Box

SIGNATURE CARE EYE DROPS HIGH PERFORMANCE 
polyethylene glycol 400, propylene glycol solution/ drops
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:21130-702
Route of AdministrationOPHTHALMIC
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
POLYETHYLENE GLYCOL 400 (UNII: B697894SGQ) (POLYETHYLENE GLYCOL 400 - UNII:B697894SGQ) POLYETHYLENE GLYCOL 4000.4 g  in 100 mL
PROPYLENE GLYCOL (UNII: 6DC9Q167V3) (PROPYLENE GLYCOL - UNII:6DC9Q167V3) PROPYLENE GLYCOL0.3 g  in 100 mL
Inactive Ingredients
Ingredient NameStrength
AMINOMETHYLPROPANOL (UNII: LU49E6626Q)  
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7)  
BORIC ACID (UNII: R57ZHV85D4)  
HYPROMELLOSES (UNII: 3NXW29V3WO)  
POTASSIUM CHLORIDE (UNII: 660YQ98I10)  
WATER (UNII: 059QF0KO0R)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
SORBITOL (UNII: 506T60A25R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:21130-702-011 in 1 BOX10/05/2018
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 DrugM01810/05/2018
Labeler - Better Living Brands LLC (009137209)
Registrant - KC Pharmaceuticals, Inc. (174450460)
Establishment
NameAddressID/FEIBusiness Operations
KC Pharmaceuticals, Inc.174450460manufacture(21130-702) , pack(21130-702) , label(21130-702)

Revised: 12/2023
Document Id: 0cfa48cc-26af-c528-e063-6394a90a3aa9
Set id: 6f1f4f58-3208-4b06-9afb-c4beeed09314
Version: 4
Effective Time: 20231220
 
Better Living Brands LLC