Touchpoint™ Hand Sanitizing Wipes Fragrance Free

Manufacturer: Innocore Sales & Marketing Inc
Effective date: 2026-07-17
Label type: HUMAN OTC DRUG LABEL
Version: 4
Source: daily-update
Hydrated at: 2026-07-21 05:10:12

Label at a glance#

ProductTouchpoint Hand Sanitizing Wipes Fragrance Free

Active ingredientBENZALKONIUM CHLORIDE

Label structure9 sections

Dosage and administration

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.

Contacts and useful links#

PhoneLabel contact1.877.910.4809

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

Drug Facts

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium Chloride 0.13

Purpose

OTC - PURPOSE SECTION

Antimicrobal

Use

INDICATIONS & USAGE SECTION

Hand sanitizer to help reduce bacteria on the skin. Recommended for repeated use.

Warnings

WARNINGS SECTION

For external use only.

OTC - WHEN USING SECTION

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

OTC - DO NOT USE SECTION

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.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children.

Directions

DOSAGE & ADMINISTRATION SECTION

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

INACTIVE INGREDIENT SECTION

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

Questions?

OTC - QUESTIONS SECTION

1.877.910.4809

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

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

PRINCIPAL DISPLAY PANEL - 320 Wipe Canister Label

DailyMed Product Concepts#

Product concept, Relation, Version table
Product concept	Relation	Version	Effective
c6f86816-7da6-43ea-8c25-ac9758311cc5	Product name	1	20220118
252e11b6-1a9a-4283-a242-df2c129c496d	Product name	3	20170717

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 10 matching rows.

Touchpoint Hand Sanitizing Wipes Fragrance Free
Benzalkonium Chloride
DEHYDROACETIC ACID
CAPRYLYL/CAPRYL OLIGOGLUCOSIDE
PHENOXYETHANOL
BENZOIC ACID
POLY(LAURYLGLUCOSIDE)-7
PROPYLENE GLYCOL
WATER
BENZALKONIUM

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
70924-003	70924-003-01, 70924-003-02, 70924-003-03, 70924-003-04

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 8 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
DEHYDROACETIC ACID	2KAG279R6R	IACT
CAPRYLYL/CAPRYL OLIGOGLUCOSIDE	E00JL9G9K0	IACT
PHENOXYETHANOL	HIE492ZZ3T	IACT
BENZOIC ACID	8SKN0B0MIM	IACT
POLY(LAURYLGLUCOSIDE)-7	VB00RDE21R	IACT
PROPYLENE GLYCOL	6DC9Q167V3	IACT
WATER	059QF0KO0R	IACT
BENZALKONIUM CHLORIDE	F5UM2KM3W7	ACTIB

Source Document#

Source XML

Older Hydrated Versions#

Version, Effective date, Source table
Version	Effective date	Source	Hydrated
3	2025-06-19	full-release	2026-06-01 01:03:31

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Touchpoint Hand Sanitizing Wipes Fragrance Free	BENZALKONIUM CHLORIDE	Innocore Sales & Marketing Inc	9886fa20-65c7-4deb-a1ae-0c3e52ba887e	2026-07-17	Warnings	Exact identifier ndc (package): 70924-003-02 ndc (package): 70924-003-04 ndc (package): 70924-003-01 ndc (package): 70924-003-03 ndc (product): 70924-003 ndc11 (package): 70924000303 ndc11 (package): 70924000302 ndc11 (package): 70924000301 ndc11 (package): 70924000304 spl id: 56d4a994-e5a3-22af-e063-6394a90a02fe spl set id: 9886fa20-65c7-4deb-a1ae-0c3e52ba887e

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.