ANTIBACTERIAL HAND SANITIZER- alcohol gel

Antibacterial Hand Sanitizer by

Drug Labeling and Warnings

Antibacterial Hand Sanitizer by is a Otc medication manufactured, distributed, or labeled by Tiege Hanley, BMC 1092, Inc. dba Solo Laboratories, Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

SPL UNCLASSIFIED SECTION

Drug Facts

Active Ingredient

Ethyl Alcohol 62%

Purpose

Antiseptic

Uses

• for hand washing to decrease bacteria on the skin
• recommended for repeated use

Warnings

For external use only.

Flammable. Keep away from fire or flame.

When using this product do not use in or around the eyes. In case of contact, rinse eyes thoroughly with water.

Stop use and ask a doctor if irritation and redness develop and persist for more than 72 hours.

If swallowed get medical help or contact poison control center right away.

Keep Out of reach of children.

Directions

• wet hands thoroughly with product
• briskly rub hands together until dry
• Supervise children in the use of this product.

Other Information

• store at 20-25° C (68 to 77°F)
• may discolor certain fabrics

Inactive Ingredients

Water, Propylene Glycol, Acrylates/C10-3- Alkyl Acrylate Crosspolymer, Peg-60, Almond Glycerides, Aloe Barbadensis Leaf Juice, Tocopheryl Acetate, Triisopropanolamine, Fragrance

SPL UNCLASSIFIED SECTION

Distributed by Tiege Hanley LLC
Chicago, IL 60612

PRINCIPAL DISPLAY PANEL - 59 mL Bottle Label

TIÉGE
HANLEY

Uncomplicated
Skin Care for Men®

HAND SANITIZER

Kills 99.99% of
All Germs

2 fl oz (59 mL)

INGREDIENTS AND APPEARANCE

ANTIBACTERIAL HAND SANITIZER 
alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 71714-059
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
alcohol (UNII: 3K9958V90M) (alcohol - UNII:3K9958V90M)	alcohol	62 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
Propylene Glycol (UNII: 6DC9Q167V3)
water (UNII: 059QF0KO0R)
PEG-60 ALMOND GLYCERIDES (UNII: 4Y0E651N0F)
aloe vera leaf (UNII: ZY81Z83H0X)
.Alpha.-Tocopherol Acetate (UNII: 9E8X80D2L0)
triisopropanolamine (UNII: W9EN9DLM98)
CARBOMER INTERPOLYMER TYPE B (ALLYL PENTAERYTHRITOL CROSSLINKED) (UNII: 132584PQMO)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 71714-059-02	59 mL in 1 BOTTLE; Type 0: Not a Combination Product	03/31/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC MONOGRAPH NOT FINAL	part333E	03/31/2020

Labeler - Tiege Hanley (080305325)

Registrant - BMC 1092, Inc. dba Solo Laboratories, Inc. (078831987)

Establishment
Name	Address	ID/FEI	Business Operations
BMC 1092, Inc. dba Solo Laboratories, Inc.		078831987	MANUFACTURE(71714-059) , LABEL(71714-059) , PACK(71714-059)