TOUCHPOINT HAND SANITIZING WIPES FRAGRANCE FREE- benzalkonium chloride cloth

Touchpoint Hand Sanitizing Wipes Fragrance Free by

Drug Labeling and Warnings

Touchpoint Hand Sanitizing Wipes Fragrance Free 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 productdo not use in or near the eyes. In case of contact, rinse eyes thoroughly in water.

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

If swallowed getmedical 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

320 Wipe Canister Label

Touch
Point™

Hand Sanitizing
Wipes

FRAGRANCE FREE

320
wipes
(6.6" x 6.75")

Kills 99.99%
of most common germs that may cause illness

INGREDIENTS AND APPEARANCE

TOUCHPOINT HAND SANITIZING WIPES FRAGRANCE FREE 
benzalkonium chloride cloth

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 70924-003
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
BENZOIC ACID (UNII: 8SKN0B0MIM)
CAPRYLYL/CAPRYL OLIGOGLUCOSIDE (UNII: E00JL9G9K0)
DEHYDROACETIC ACID (UNII: 2KAG279R6R)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
POLY(LAURYLGLUCOSIDE)-7 (UNII: VB00RDE21R)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 70924-003-01	320 in 1 CANISTER; Type 0: Not a Combination Product	09/24/2020
2	NDC: 70924-003-02	500 in 1 BAG; Type 0: Not a Combination Product	09/24/2020
3	NDC: 70924-003-03	1500 in 1 BAG; Type 0: Not a Combination Product	09/24/2020
4	NDC: 70924-003-04	320 in 1 POUCH; Type 0: Not a Combination Product	09/24/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	505G(a)(3)	09/24/2020

Labeler - Innocore Sales & Marketing Inc (201152597)