ARTIFICIAL TEARS- polyvinyl alcohol solution/ drops 
Aru Pharma Inc.

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.

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QPACK ARTIFICIAL TEARS

Drug Facts

Active Ingredient

Polyvinyl Alcohol 1.4%

Purpose

Eye Lubricant

Uses

Warnings

Do not use

When using this product

Stop use and ask a doctor

Keep out of reach of children

  • if swallowed, get medical help or contact a poison control center right away.

Question or comments?

1-844-500-2729

between 9 am and 4 pm EST, Monday-Friday.

Directions

Instill 1 or 2 drops in the affected eye(s) as needed.

Other information

Inactive Ingredients

benzalkonium chloride, dibasic sodium phosphate hydrate, edetate disodium hydrate, monobasic sodium phosphate dihydrate, purified water, sodium chloride

Compare to the active Ingredient in Liquifilm Tears Eye Drops

Lubricant Eye Drops

Prevents Irritation and Relieves Dryness of the eye

Distributed by.

ARU PARMA INC.

MOUNT VERNON, NY 10552

www.qpackrx.com

Packaging

Qpack1

ARTIFICIAL TEARS 
polyvinyl alcohol solution/ drops
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:70403-920
Route of AdministrationOPHTHALMIC
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
POLYVINYL ALCOHOL, UNSPECIFIED (UNII: 532B59J990) (POLYVINYL ALCOHOL, UNSPECIFIED - UNII:532B59J990) POLYVINYL ALCOHOL, UNSPECIFIED14 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7)  
SODIUM PHOSPHATE, DIBASIC, DODECAHYDRATE (UNII: E1W4N241FO)  
EDETATE DISODIUM (UNII: 7FLD91C86K)  
SODIUM PHOSPHATE, MONOBASIC, DIHYDRATE (UNII: 5QWK665956)  
WATER (UNII: 059QF0KO0R)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:70403-920-151 in 1 CARTON03/31/202003/31/2025
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 finalpart34903/31/202003/31/2025
Labeler - Aru Pharma Inc. (079736192)

Revised: 5/2023
Document Id: 6eb34145-5774-4fda-8120-6feb6c58bd47
Set id: 9339a60f-0bf2-4d3e-860f-ef8e9c6cea98
Version: 2
Effective Time: 20230515
 
Aru Pharma Inc.