SANIRUS HAND SANITIZER- alcohol gel

Sanirus Hand Sanitizer by

Drug Labeling and Warnings

Sanirus Hand Sanitizer by is a Otc medication manufactured, distributed, or labeled by 6A Holding, LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient

Ethyl Alcohol 70% v/v

Purpose

Antiseptic

Use

Hand Sanitizer to help decrease bacteria on the skin. 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 eye contact immediately flush eyes throughly 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

In case of accidental ingestion, contact a doctor or Poison Control Center immediately.

Directions

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

Other information

■ Store between 15-30C (59-89F) ■ Avoid freezing and excessive heat above 40C (104F) ■ May discolor fabrics or surfaces

Inactive ingredients

Aloe vera leaf, Aminomethylpropanol, Carbomer, Gycerin, Propylene Glycol, Tocopherol Acetate, Water

Package Label

INGREDIENTS AND APPEARANCE

SANIRUS HAND SANITIZER 
alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 74691-001
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
GLYCERIN (UNII: PDC6A3C0OX)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
WATER (UNII: 059QF0KO0R)
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)
AMINOMETHYLPROPANOL (UNII: LU49E6626Q)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 74691-001-12	355 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	04/13/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	04/13/2020

Labeler - 6A Holding, LLC (117474000)