RELIANT HAND SANITIZING GEL- ethyl alcohol gel

RELIANT Hand Sanitizing Gel by

Drug Labeling and Warnings

RELIANT Hand Sanitizing Gel by is a Otc medication manufactured, distributed, or labeled by Procurement Services LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

SPL UNCLASSIFIED SECTION

Drug Facts

ACTIVE INGREDIENT

Active ingredient[s]

Ethyl Alcohol 72%

PURPOSE

Purpose

Antiseptic

INDICATIONS & USAGE

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

WARNINGS

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

DO NOT USE

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

WHEN USING

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

STOP USE

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

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

DOSAGE & ADMINISTRATION

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 SAFETY INFORMATION

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

INACTIVE INGREDIENT

Inactive ingredients  Water, carbomer, glycerin,
triethanolamine, hydrogen peroxide.

Package Labeling -  Principal Display Panel

HAND

SANITIZING GEL

Kills 99.9% of Germs

Clinically-tested

Hospital-trusted

RELIANT

Unscented

33.8 OZ (1L)

Distributed by
Procurement Services LLC
Nashville, TN 37215
+1 (615) 345-2544
www.my-reliant.com

PRODUCT OF MEXICO

NDC: 74882-831-01

8  60003 64606  9

1 Liter Bottle

500 mL Bottle

200mL Bottle

res

INGREDIENTS AND APPEARANCE

RELIANT HAND SANITIZING GEL 
ethyl alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 74882-831
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	72 L  in 100 L

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)
GLYCERIN (UNII: PDC6A3C0OX)
TROLAMINE (UNII: 9O3K93S3TK)
HYDROGEN PEROXIDE (UNII: BBX060AN9V)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 74882-831-01	1 L in 1 BOTTLE; Type 0: Not a Combination Product	07/29/2020
2	NDC: 74882-831-02	0.5 L in 1 BOTTLE; Type 0: Not a Combination Product	07/29/2020
3	NDC: 74882-831-03	0.2 L in 1 BOTTLE; Type 0: Not a Combination Product	07/29/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	07/29/2020

Labeler - Procurement Services LLC (117471256)

Registrant - Procurement Services LLC (117471256)