HEB LUBRICANT EYE DROPS DRY EYE THERAPY- propylene glycol solution/ drops 
HEB

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HEB Lubricant Eye Drops Dry Eye Therapy 15mL and 15mL twin pack (PLD)

Active ingredient

Propylene glycol 0.6%

Purpose

Lubricant

Use

Warnings

For external use only.

Do not use

  • if this product changes color
  • if you are sensative to any ingredient in this product

When using this product

  • do not touch tip of container to any surface to avoid contamination
  • replace cap after each use

Stop use and ask a doctor if

  • you experience eye pain
  • changes in vision occur
  • redness or irritation of the eye(s) gets worse, persists or lasts 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

Other information

Inactive ingredients

benzalkonium chloride, boric acid, castor oil, disodium edetate hydrate, **hydrochloric acid, polyoxyethylene sorbitan monooleate, potassium chloride, purified water, sodium borate, sodium chloride, **sodium hydroxide

**May contain these ingredients to adjust pH.

HEB Lubricant Eye Drops Dry Eye Therapy 15mL

HEB Lubricant Eye Drops Dry Eye Therapy 15mL

HEB Lubricant Eye Drops Dry Eye Therapy 15mL twin pack

HEB Lubricant Eye Drops Dry Eye Therapy 15mL twin pack

HEB LUBRICANT EYE DROPS DRY EYE THERAPY 
propylene glycol solution/ drops
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:37808-650
Route of AdministrationOPHTHALMIC
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
PROPYLENE GLYCOL (UNII: 6DC9Q167V3) (PROPYLENE GLYCOL - UNII:6DC9Q167V3) PROPYLENE GLYCOL0.6 g  in 100 mL
Inactive Ingredients
Ingredient NameStrength
BORIC ACID (UNII: R57ZHV85D4)  
CASTOR OIL (UNII: D5340Y2I9G)  
PEG-6 SORBITAN OLEATE (UNII: 58O7V09UCI)  
POTASSIUM CHLORIDE (UNII: 660YQ98I10)  
WATER (UNII: 059QF0KO0R)  
SODIUM BORATE (UNII: 91MBZ8H3QO)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7)  
EDETATE DISODIUM (UNII: 7FLD91C86K)  
SODIUM HYDROXIDE (UNII: 55X04QC32I)  
HYDROCHLORIC ACID (UNII: QTT17582CB)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:37808-650-011 in 1 BOX09/12/2020
115 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product
2NDC:37808-650-022 in 1 BOX09/12/2020
215 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 DrugM01809/12/2020
Labeler - HEB (007924756)
Registrant - KC Pharmaceuticals, Inc. (174450460)
Establishment
NameAddressID/FEIBusiness Operations
Daewoo Pharmaceutical Co., Ltd.689046329manufacture(37808-650) , pack(37808-650) , label(37808-650)

Revised: 12/2023
Document Id: 0cfaa641-21fc-e11b-e063-6394a90a69f2
Set id: af29a7a2-7c07-f3ec-e053-2a95a90ac845
Version: 2
Effective Time: 20231220
 
HEB