Touchpoint Biodegradable Sanitizing Wipes: Package Insert and Label Information

TOUCHPOINT BIODEGRADABLE SANITIZING WIPES- benzalkonium chloride cloth
Innocore Sales & Marketing Inc

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

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

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TOUCHPOINT BIODEGRADABLE SANITIZING WIPES
benzalkonium chloride cloth
Product Information
Product Type HUMAN OTC DRUG Item Code (Source) NDC:70924-004
Route of Administration CUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
BENZALKONIUM CHLORIDE (BENZALKONIUM) BENZALKONIUM CHLORIDE 1.3 mg
Inactive Ingredients
Ingredient Name Strength
WATER
PROPYLENE GLYCOL
CAPRYLYL/CAPRYL OLIGOGLUCOSIDE
POLY(LAURYLGLUCOSIDE)-7
PHENOXYETHANOL
BENZOIC ACID
DEHYDROACETIC ACID
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:70924-004-02 2 POUCH in 1 BOX contains a POUCH (70924-004-01)
1 NDC:70924-004-01 840 CLOTH in 1 POUCH This package is contained within the BOX (70924-004-02)
2 NDC:70924-004-04 6 CANISTER in 1 BOX contains a CANISTER (70924-004-03)
2 NDC:70924-004-03 1000 CLOTH in 1 CANISTER This package is contained within the BOX (70924-004-04)
3 NDC:70924-004-06 2 POUCH in 1 BOX contains a POUCH (70924-004-05)
3 NDC:70924-004-05 1200 CLOTH in 1 POUCH This package is contained within the BOX (70924-004-06)
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
OTC monograph not final part333E 01/01/2022
Labeler — Innocore Sales & Marketing Inc (201152597)

Revised: 01/2022 Innocore Sales & Marketing Inc

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