SANIRUS HAND SANITIZER- ethyl 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]

Drug Facts

Active Ingredients

Ethyl Alcohol 65% v/v

Purpose

Antiseptic

INDICATIONS & USAGE

Uses: Hand Sanitizer to help reduce bacteria on skin

WARNINGS

Warnings: For external use only.

Flammable. keep away from heat or flame.

When using this product Avoid contact with eyes. In case of contact rinse with water.  Do not inhale or ingest. Avoid contact with broken skin.

Stop use and ask a doctor if skin irritation develops.

Keep out of reach of children. In case of accidental ingestion, get medical help or contact a Poison Control Center immediately

DOSAGE & ADMINISTRATION

Directions Wet hands thoroughly and rub together until dry. Adult supervision for children under 6. Not for infants.

STORAGE AND HANDLING

Other information Store between 15°-30°C (59°-86°F). May discolor fabrics

INACTIVE INGREDIENT

Inactive Ingredients: Water (Aqua), Butylene Glycol, Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Aloe Barbadensis Leaf Juice, Triethanolamine, Citric Acid.

SPL UNCLASSIFIED SECTION

KILLS MOST OF THE GERMS

65% ALCOHOL

ALOE VERA

2X SANITIZING STRENGTH

REFRESHING GEL

GMP Quality

DISTRIBUTED BY: 6A HOLDING LLC, MIAMI, FLORIDA

MADE IN CHINA

Packaging

INGREDIENTS AND APPEARANCE

SANIRUS HAND SANITIZER 
ethyl alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 74691-002
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	65 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED) (UNII: 59TL3WG5CO)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
TROLAMINE (UNII: 9O3K93S3TK)
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 74691-002-02	60 mL in 1 BOTTLE; Type 0: Not a Combination Product	04/23/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	04/23/2020

Labeler - 6A Holding, LLC (117474000)