ARCHIES DRY EYE RELIEF- polyethylene glycol 400, propylene glycol solution/ drops 
Archie's Remedies

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Archie's Dry Eye Relief 30ct & 60ct (PLD)

Active ingredients

Polyethylene glycol 400 0.4%

Propylene glycol 0.3%

Purposes

Lubricant

Lubricant

Use

Warnings

For external use only

Do not use

  • if this solution changes color or becomes cloudy
  • if you are sensitive to any ingredient in this product

When using this product

  • to avoid contamination, do not touch tip of container to any surface.
  • do not reuse. Once opened, discard.

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

Other information

Inactive ingredients

boric acid, hypromellose, potassium chloride, purified water, sodium chloride. May contain hydrochloric acid and/or sodium hydroxide to adjust pH.

Archie's Dry Eye Relief 30ct

Archie's Dry Eye Relief 30ct

Archie's Dry Eye Relief 60ct

Archie's Dry Eye Relief 60ct

ARCHIES DRY EYE RELIEF 
polyethylene glycol 400, propylene glycol solution/ drops
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:83737-001
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
POTASSIUM CHLORIDE (UNII: 660YQ98I10)  
WATER (UNII: 059QF0KO0R)  
HYDROCHLORIC ACID (UNII: QTT17582CB)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
HYPROMELLOSE, UNSPECIFIED (UNII: 3NXW29V3WO)  
SODIUM HYDROXIDE (UNII: 55X04QC32I)  
BORIC ACID (UNII: R57ZHV85D4)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:83737-001-3030 in 1 BOX10/16/2023
10.4 mL in 1 VIAL, SINGLE-USE; Type 0: Not a Combination Product
2NDC:83737-001-6060 in 1 BOX10/16/2023
20.4 mL in 1 VIAL, SINGLE-USE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM01810/16/2023
Labeler - Archie's Remedies (118986599)
Registrant - KC Pharmaceuticals, Inc. (174450460)
Establishment
NameAddressID/FEIBusiness Operations
Unimed Pharmaceuticals, Inc.689852052manufacture(83737-001) , pack(83737-001) , label(83737-001)

Revised: 11/2023
Document Id: 0a38e951-4cfa-71bf-e063-6294a90a995f
Set id: 07da099b-6b7f-984d-e063-6294a90a12ac
Version: 2
Effective Time: 20231115
 
Archie's Remedies