PRO+CURE HAND SANITIZING GEL

PRO CURE HAND SANITIZING by

Drug Labeling and Warnings

PRO CURE HAND SANITIZING by is a Otc medication manufactured, distributed, or labeled by Procurement Services LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

PRO CURE HAND SANITIZING- ethyl alcohol gel 
Procurement Services LLC

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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PRO+CURE HAND SANITIZING GEL

Drug Facts

Active ingredient[s]

Ethyl Alcohol 70%

Purpose

Antiseptic

Use[s]
Hand sanitizer to help reduce bacteria that potentially
can cause disease. For use when soap and water are not available.

Warnings
■ For external use only. Flammable.
■ Keep away from heat or flame.

Do not use
■ In children less than 2 months of age
■ On open skin wounds

When using this product keep out of eyes, ears, and mouth.
In case of contact with eyes, rinse eyes thoroughly with water.

Stop use and ask a doctor if irritation or rash occurs.
These may be signs of a serious condition.

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

Directions
■ Place enough product on hands to cover all surfaces.
  Rub hands together until dry.
■ Supervise children under 6 years of age when using this
  product to avoid swallowing.

Other information
■ Store between 15-30C (59-86F)
■ Avoid freezing and excessive heat above 40C (104F)

Inactive ingredients  Water, carbomer, glycerin,
triethanolamine.

Package Labeling

HAND

SANITIZING GEL

Kills 99.9% of Germs

Clinically-tested

Hospital-trusted

PRO+CURE

Unscented

33.8 OZ (1L)

Distributed by
Procurement Services LLC
Nashville, TN 37215
+1 (615) 345-2544
www.pro-cure.io

PRODUCT OF MEXICO

NDC: 74882-469-01

8  60003 64603  8

1 Liter Bottle

500 mL Bottle

200mL Bottle

res

PRO CURE HAND SANITIZING 
ethyl alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 74882-469
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	70 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)
GLYCERIN (UNII: PDC6A3C0OX)
TROLAMINE (UNII: 9O3K93S3TK)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 74882-469-01	1000 mL in 1 BOTTLE; Type 0: Not a Combination Product	04/17/2020	04/17/2020
2	NDC: 74882-469-02	500 mL in 1 BOTTLE; Type 0: Not a Combination Product	04/17/2020	04/17/2020
3	NDC: 74882-469-03	200 mL in 1 BOTTLE; Type 0: Not a Combination Product	04/17/2020	04/17/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	04/17/2020	04/17/2020

Labeler - Procurement Services LLC (117471256)

Registrant - Procurement Services LLC (117471256)

Revised: 6/2020

Document Id: 4e0d0ab2-ccdd-482e-ab7d-0213642f7916

34390-5

Set id: 71c6ecae-d201-466b-a2d5-a7468da90b62

Version: 2

Effective Time: 20200616