TOUCHPOINT WIPES FRAGRANCE FREE SANITIZING WIPES- benzalkonium chloride cloth

Touchpoint Wipes Fragrance Free by

Drug Labeling and Warnings

Touchpoint 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 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.
• Children under 6 years of age should be supervised when using this product.
• Be sure to use entire wipe.
• Discard after single use.

Inactive ingredients

Water, propylene glycol, decyl/lauryl glucoside, glucoside, phenoxyethanol, benzoic acid, dehydroacetic acid.

PRINCIPAL DISPLAY PANEL - 2 Roll Case Label

Touchpoint
wipes

FRAGRANCE FREE
Kills 99.99%
of most common germs
that may cause illness

Sanitizing
wipes

1500
count

Premium fabric quickly
removes dirt and soil

INGREDIENTS AND APPEARANCE

TOUCHPOINT WIPES FRAGRANCE FREE   SANITIZING WIPES
benzalkonium chloride cloth

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 70924-002
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)
LAURYL GLUCOSIDE (UNII: 76LN7P7UCU)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
BENZOIC ACID (UNII: 8SKN0B0MIM)
DEHYDROACETIC ACID (UNII: 2KAG279R6R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 70924-002-02	2 in 1 BOX	09/09/2016
1	NDC: 70924-002-01	1500 in 1 POUCH; Type 0: Not a Combination Product
2	NDC: 70924-002-04	2 in 1 BOX	12/11/2018
2	NDC: 70924-002-03	1800 in 1 POUCH; Type 0: Not a Combination Product
3	NDC: 70924-002-06	2 in 1 BOX	12/11/2018
3	NDC: 70924-002-05	2400 in 1 POUCH; Type 0: Not a Combination Product
4	NDC: 70924-002-09	2 in 1 BOX	12/11/2018
4	NDC: 70924-002-07	400 in 1 POUCH; Type 0: Not a Combination Product
5	NDC: 70924-002-11	6 in 1 BOX	12/11/2018
5	NDC: 70924-002-10	320 in 1 CANISTER; Type 0: Not a Combination Product
6	NDC: 70924-002-13	6 in 1 BOX	10/16/2019
6	NDC: 70924-002-12	150 in 1 CANISTER; Type 0: Not a Combination Product
7	NDC: 70924-002-15	2 in 1 BOX	11/11/2019
7	NDC: 70924-002-14	2200 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 NOT FINAL	part333E	09/09/2016

Labeler - Innocore Sales & Marketing Inc (201152597)