DRPURX HAND SANITIZER- alcohol gel 
Loom USA

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.

----------

DrPuRx HAND SANITIZER

Drug Facts

Active Ingredients

Ethyl Alcohol 70%

Purpose

Antimicrobial

Uses

Warnings

For external use only: hands

Flammable, keep away from fire or flame

When using this product

  • keep out of eyes. In case of contact with eyes, flush thoroughly with water.
  • avoid contact with broken skin
  • do not inhale or ingest.

Stop use and ask a doctor if

  • irritation and redness develop
  • condition persists for more than 72 hours

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away

Directions

Other information

Inactive ingredients

water, acrylates/C10-30 alkyl acrylate crosspolymer, sodium PCA, hyaluronic acid

Distributed by:
LoomUSA LLC
3 Graphics Dr
Ewing, NJ 08628

Manufactured by:
LoomUSA LLC
FDA Registered Facility

PRINCIPAL DISPLAY PANEL - 499.79 mL Bottle Label

Made in
the USA

DrPuRX

HAND SANITIZER

Kills more than 99% of infectious agents*

Moisturizers leavehands smooth

16.9 FL OZ (499.79mL)

Principal Display Panel - 499.79 mL Bottle Label
DRPURX HAND SANITIZER 
alcohol gel
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:80607-921
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL70 mL  in 100 mL
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED) (UNII: 59TL3WG5CO)  
SODIUM PYRROLIDONE CARBOXYLATE (UNII: 469OTG57A2)  
HYALURONIC ACID (UNII: S270N0TRQY)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:80607-921-01250 mL in 1 BOTTLE; Type 0: Not a Combination Product03/01/2020
2NDC:80607-921-02500 mL in 1 BOTTLE; Type 0: Not a Combination Product03/01/2020
3NDC:80607-921-0350 mL in 1 BOTTLE; Type 0: Not a Combination Product03/01/2020
4NDC:80607-921-04118.2 mL in 1 BOTTLE; Type 0: Not a Combination Product03/01/2020
5NDC:80607-921-053785.4 mL in 1 BOTTLE; Type 0: Not a Combination Product03/01/2020
6NDC:80607-921-06208197.65 mL in 1 DRUM; Type 0: Not a Combination Product03/25/2020
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC MONOGRAPH NOT FINALpart333A03/01/2020
Labeler - Loom USA (117514119)
Establishment
NameAddressID/FEIBusiness Operations
LoomUSA LLC117514119MANUFACTURE(80607-921)

Revised: 8/2022
Document Id: f1a708cc-db5e-4a28-8f70-3d1a97e5ee1a
Set id: 959e4f6e-9ef0-401f-b4b5-eefceb5010f0
Version: 3
Effective Time: 20220802
 
Loom USA