TOUCHPOINT BIODEGRADABLE SANITIZING WIPES- benzalkonium chloride cloth

Touchpoint Biodegradable Sanitizing Wipes by

Drug Labeling and Warnings

Touchpoint Biodegradable Sanitizing Wipes by is a Otc medication manufactured, distributed, or labeled by Innocore Sales & Marketing Inc. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

SPL UNCLASSIFIED SECTION

Drug Facts

Active ingredient

Benzalkonium Chloride 0.13 %

Purpose

Antimicrobal

Use

Hand sanitizer to help reduce bacteria on the skin.

Recommended for repeated use.

Warnings

For external use only.

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

Discontinue use if irritation and redness develop. If conditions persist for more than 72 hours, consult a physician.

If swallowed get medical help or contact a poison control center immediately.

Keep out of reach of children.

Directions

• Wet hands thoroughly with product and allow to dry.
• Be sure to use entire wipe.
• Discard after single use.
• Children under 6 years of age should be supervised when using this product.

Inactive ingredients

Benzoic Acid, Caprylyl/Capryl Oligoglucoside, Dehydroacetic Acid, Phenoxyethanol, Poly(Laurylglucoside)-7, Propylene Glycol, Water

Questions?

1.877.910.4809

PRINCIPAL DISPLAY PANEL

Touch
Point TM

Biodegradable

Sanitizing Wipes

840 Wipes

Fragrance Free

Kills 99.99% of most common germs that may cause illness

OPENING DIRECTIONS

1

Keep roll in pouch and tear

open hole at top of pouch

2

Remove plastic tube.

3

Pull first wipe from centre

of roll up through

opening of package

OR

4

Thread first wipe up through dispenser

nozzle in lid of floor model.

Thread first wipe up through dispenser

nozzle in lid of wall-mounted model.

WB840FF (8" x 5")

TouchPointWipes.com
Touch Point Wipes Produced by:
Innocore - Woodstock, Ontario, Canada N4T 0K9
MADE IN CANADA

INGREDIENTS AND APPEARANCE

TOUCHPOINT BIODEGRADABLE SANITIZING WIPES 
benzalkonium chloride cloth

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 70924-004
Route of Administration	CUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)	BENZALKONIUM CHLORIDE	1.3 mg

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
CAPRYLYL/CAPRYL OLIGOGLUCOSIDE (UNII: E00JL9G9K0)
POLY(LAURYLGLUCOSIDE)-7 (UNII: VB00RDE21R)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
BENZOIC ACID (UNII: 8SKN0B0MIM)
DEHYDROACETIC ACID (UNII: 2KAG279R6R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 70924-004-02	2 in 1 BOX	01/01/2022
1	NDC: 70924-004-01	840 in 1 POUCH; Type 0: Not a Combination Product
2	NDC: 70924-004-04	6 in 1 BOX	01/01/2022
2	NDC: 70924-004-03	1000 in 1 CANISTER; Type 0: Not a Combination Product
3	NDC: 70924-004-06	2 in 1 BOX	01/01/2022
3	NDC: 70924-004-05	1200 in 1 POUCH; 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)	01/01/2022

Labeler - Innocore Sales & Marketing Inc (201152597)