RHINO HAND SANITIZING WIPES- benzalkonium chloride cloth

RHINO Hand Sanitizing Wipes by

Drug Labeling and Warnings

RHINO Hand Sanitizing Wipes by is a Otc medication manufactured, distributed, or labeled by Tazza Brands East, Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

SPL UNCLASSIFIED SECTION

Drug Facts

ACTIVE INGREDIENT

Active ingredient

Benzalkonium chloride 0.13%

PURPOSE

Purpose

Antimicrobial

INDICATIONS & USAGE

Uses

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

WARNINGS

Warnings

For external use only

When using this product avoid contact with the eyes. In case of contact, flush eyes thoroughly with water.

Stop use and ask a doctor if irritation or redness develop or last more than 72 hours.

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

DOSAGE & ADMINISTRATION

Directions

• take wipe and rub thoroughly over all surfaces of both hands
• rub hands together briskly to dry
• dispose of wipe in trash; do not fliush

INACTIVE INGREDIENT

Inactive ingredients Aqua, Aloe Barbadensis Leaf Juice, Decyl Glucoside, Glycerin, Fragrance

SPL UNCLASSIFIED SECTION

Made in China

Manufactured for:

Tazza Brands East, Inc.

2232 Dell Range Blvd

Suite 202

Cheyenne, WY 82009

PRINCIPAL DISPLAY PANEL

RHINO WIPES

Benzalkonium Chloride 0.13%

HAND SANITIZING WIPES

1500 Wet Wipes

5 in. x 8 in. (13cm x 20cm)

Alcohol Free

INGREDIENTS AND APPEARANCE

RHINO HAND SANITIZING WIPES 
benzalkonium chloride cloth

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 76370-0026
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)	BENZALKONIUM CHLORIDE	0.13 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
GLYCERIN (UNII: PDC6A3C0OX)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
DECYL GLUCOSIDE (UNII: Z17H97EA6Y)
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 76370-0026-0	1500 in 1 POUCH	07/16/2024
1		1.3 mL in 1 APPLICATOR; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	505G(a)(3)	07/16/2024

Labeler - Tazza Brands East, Inc. (117842371)