HYDRATE LUBRICANT- polyethylene glycol 400 and propylene glycol solution/ drops 
Sproose Products Inc.

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HYDRATE Lubricant

Drug Facts

Active Ingredients Purposes
Polyethylene glycol 400 0.04%Lubricant
Propylene glycol 0.3%Lubricant

Uses

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

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

Stop use and ask a doctor if you experience any of the following

  • eye pain
  • changes in vision
  • continued redness or irritation of the eye
  • the condition worsens or persists 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

Other information

store at 15°-30°C (59°-86°F)

Inactive Ingredients

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

Questions?

866-778-0043 Alchemy43.com

Distributed by
Sproose Products Inc.
West Hollywood, CA

PRINCIPAL DISPLAY PANEL - 15 mL Bottle Carton

ALCHEMY 43

HYDRATE

LUBRICANT
EYE DROPS

STERILE 0.5 FL. OZ (15mL)

PRINCIPAL DISPLAY PANEL - 15 mL Bottle Carton
HYDRATE LUBRICANT 
polyethylene glycol 400 and propylene glycol solution/ drops
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:83716-6000
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
POLYETHYLENE GLYCOL 400 (UNII: B697894SGQ) (POLYETHYLENE GLYCOL 400 - UNII:B697894SGQ) POLYETHYLENE GLYCOL 4000.004 g  in 1 mL
PROPYLENE GLYCOL (UNII: 6DC9Q167V3) (PROPYLENE GLYCOL - UNII:6DC9Q167V3) PROPYLENE GLYCOL0.003 g  in 1 mL
Inactive Ingredients
Ingredient NameStrength
AMINOMETHYLPROPANOL (UNII: LU49E6626Q)  
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7)  
BORIC ACID (UNII: R57ZHV85D4)  
HYPROMELLOSE, UNSPECIFIED (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:83716-6000-11 in 1 CARTON09/01/2023
115 mL in 1 BOTTLE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph drugM01809/01/2023
Labeler - Sproose Products Inc. (119019937)
Establishment
NameAddressID/FEIBusiness Operations
Samson Pharmaceuticals Inc.088169581MANUFACTURE(83716-6000)

Revised: 3/2024
Document Id: 30a20e36-ee78-4302-8424-1dd1029ba41d
Set id: 692561b4-0102-4aa7-b818-8e787b8c1e6e
Version: 1
Effective Time: 20240308
 
Sproose Products Inc.