RELIEF CHEMISTRY HAND SANITIZER- ethyl alcohol gel

Relief Chemistry Hand Sanitizer by

Drug Labeling and Warnings

Relief Chemistry Hand Sanitizer by is a Otc medication manufactured, distributed, or labeled by FGD, LLC, Goodwin Co.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active ingredient

Ethyl Alcohol 70%

Purpose

Antimicrobial

Uses

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. Highly flammable liquid and vapor. Causes serious eye irritation. 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

When using this product avoid contact with eyes, ears, and mouth.

In case of contact with eyes, rinse eyes thoroughly with water.

Stop use or ask a doctor if

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 (1-800-222-1222) right away.

Directions

• Place enough amount 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 15-30 0C (59-86 0F)
• Avoid freezing and excessive heat above 40 0C (104 0F)

Inactive ingredients

hydroxypropyl guar, water, citric acid.

Relief Chemistry Hand Sanitizer jaguar 1 gal

INGREDIENTS AND APPEARANCE

RELIEF CHEMISTRY HAND SANITIZER 
ethyl alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 73787-121
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)
GUARAPROLOSE (1300 MPA.S AT 1%) (UNII: 1530WMS90S)
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 73787-121-01	3785 mL in 1 BOTTLE; Type 0: Not a Combination Product	06/11/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333E	06/11/2020

Labeler - FGD, LLC (111927555)

Establishment
Name	Address	ID/FEI	Business Operations
Goodwin Co.		806987483	manufacture(73787-121)