Clean and Soft Moisturizing Hand Sanitizer

Clean and Soft Moisturizing Hand Sanitizer by

Drug Labeling and Warnings

Clean and Soft Moisturizing Hand Sanitizer by is a Otc medication manufactured, distributed, or labeled by Method Pharmaceuticals, LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

CLEAN AND SOFT MOISTURIZING HAND SANITIZER- alcohol gel 
Method Pharmaceuticals, 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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Clean and Soft Moisturizing Hand Sanitizer

Clean & Soft Moisturizing Hand Sanitizer

Drug Facts

Active ingredient

Purpose

Ethyl alcohol 70% v/v..................... Antimicrobial

Uses

Hand sanitizer to help reduce bacteria on the skin

Warnings

Flammable. Keep away from fire or flame.

For external use only

When using this product

do not use in or near the eyes. In case of contact, rinse eyes thoroughly with water.

Stop use and ask a doctor if

irritation or rash appears and lasts

Keep out of reach of children.

If swallowed, get medical help or contact a Poison Control right away.

Directions

• Place enough product in your palm to thoroughly cover hands and rub hands together briskly until dry

• Children under 6 years of age should be supervised when using this product

Other information

• Store below 110°F (43°C)
  
• May discolor certain fabrics or surfaces

Inactive ingredients

Isopropyl Alcohol, Aloe Vera, Carbomer, Glycerin, Panthenol, Propanediol, Tocopherol Acetate, Triethanolamine, Water

Method Pharmaceuticals, LLC

Fort Worth, TX 76118

www.methodpharm.com

1-877-250-3427

Product Made In U.S.A.

Store below 110°F (43°C)

PRINCIPAL DISPLAY PANEL

Clean & Soft
Moisturizing Hand Sanitizer
Kills 99.9% of Germs
4 fl oz (120 mL)

CLEAN AND SOFT MOISTURIZING HAND SANITIZER 
alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 58657-595
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
ISOPROPYL ALCOHOL (UNII: ND2M416302)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)
GLYCERIN (UNII: PDC6A3C0OX)
PANTHENOL (UNII: WV9CM0O67Z)
PROPANEDIOL (UNII: 5965N8W85T)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
TROLAMINE (UNII: 9O3K93S3TK)
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 58657-595-04	120 mL in 1 BOTTLE; Type 0: Not a Combination Product	06/10/2020	12/31/2021

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333E	06/10/2020	12/31/2021

Labeler - Method Pharmaceuticals, LLC (060216698)

Revised: 12/2021

Document Id: d4749043-8bcb-3438-e053-2a95a90a8eb2

34390-5

Set id: cd0b712b-8851-48ab-a5ed-55423850fc30

Version: 3

Effective Time: 20211231