RELIEF C HAND SANITIZER UNSCENTED FOR PROFESSIONALS- ethyl alcohol gel

Relief C Hand Sanitizer Unscented for Professionals by

Drug Labeling and Warnings

Relief C Hand Sanitizer Unscented for Professionals 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 can potentially 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

• on children less than 2 months of age
• on open skin wounds

WHEN USING

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

STOP USE

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 hit produce to avoid swallowing.

OTHER SAFETY INFORMATION

• Store between 15-30 oC (59-86 oF)
• Avoid freezing and excessive heat 40 oC (104 oF)

Inactive ingredients

Glycerin, PEG-6 (and) AMP-Acrylate/vinyl-Isodecanoate Crosspolymer, Propylene-glycol, Purified Water

Relief C Hand Sanitizer Unscented for Professionals 8 oz jaguar

INGREDIENTS AND APPEARANCE

RELIEF C HAND SANITIZER UNSCENTED FOR PROFESSIONALS 
ethyl alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 73787-120
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
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
WATER (UNII: 059QF0KO0R)
GUARAPROLOSE (1300 MPA.S AT 1%) (UNII: 1530WMS90S)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 73787-120-01	236 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(73787-120)