ANTIBACTERIAL HAND SANITIZER- ethyl alcohol spray

Antibacterial Hand Sanitizer by

Drug Labeling and Warnings

Antibacterial Hand Sanitizer by is a Otc medication manufactured, distributed, or labeled by Broder Bros Co.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug Facts

Active ingredient

Ethyl Alcohol 62%

Purpose

Antiseptic

Uses

For hand sanitizing

Warnings

• Flammable.Keep away from heat and flame.
• For external use only.

When using this product

• Keep out of eyes
• In case of contact with eyes, flush thoroughly with water
• Avoid contact with broken skin
• Do not inhale or ingest

Stop use and ask a doctor

if irritation and redness develops and persists for more than 72 hours

Keep out of reach of children

If swallowed get medical help or call a Poison Control Center right away

Directions

• Wet hands thoroughly with product, briskly rub together until dry.
• Always supervise children in use of this product.
• Children under 6 months of age: Ask a doctor.

Other information

Store at 66° to 77° F (22° to 25° C)

Inactive ingredients

Aloe Barbadensis Leaf Extract, Carbomer, Deionizer Water, Fragrance, Glycerin, Propylene Glycol, Tocopherol Acetate, Triethanolamine

Questions?

1-800-873-7746 M-F 8 am - 5 pm EST

SPL UNCLASSIFIED SECTION

Net wt. 10 mL/0.33 fl. oz.

Made in China

Dist. By Broder Bros Co., dba Prime Line

Gaffney, SC 29341

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

ANTIBACTERIAL HAND SANITIZER 
ethyl alcohol spray

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 71513-202
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
TROLAMINE (UNII: 9O3K93S3TK)
WATER (UNII: 059QF0KO0R)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)
GLYCERIN (UNII: PDC6A3C0OX)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
ALOE VERA LEAF (UNII: ZY81Z83H0X)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 71513-202-30	10 mL in 1 BOTTLE; Type 0: Not a Combination Product	11/17/2025
2	NDC: 71513-202-31	20 mL in 1 BOTTLE; Type 0: Not a Combination Product	11/17/2025

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	505G(a)(3)	11/17/2025

Labeler - Broder Bros Co. (107044246)