FDA.reportPublic FDA data

Touchpoint Wipes Fragrance Free

Manufacturer
Innocore Sales & Marketing Inc
Effective date
2026-07-17
Label type
HUMAN OTC DRUG LABEL
Version
11
Source
daily-update
Hydrated at
2026-07-21 05:10:07

Label at a glance#

ProductTouchpoint Wipes Fragrance Free Sanitizing Wipes
Active ingredientBENZALKONIUM CHLORIDE
Label structure8 sections

Dosage and administration

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.

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

OTC - STOP USE SECTION

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

SPL UNCLASSIFIED SECTION

If swallowed get medical 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.
  • 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

INACTIVE INGREDIENT SECTION

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

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Touch

Point™

Sanitizing Wipes

1500 Wipes • 8"x 6"

Fragrance Free

Kills 99.99%

of most common germs that may cause illness

PRINCIPAL DISPLAY PANEL - 1500 Wipe Pouch LabelPRINCIPAL DISPLAY PANEL - 1500 Wipe Pouch Label

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
c6f86816-7da6-43ea-8c25-ac9758311cc5Product name120220118
252e11b6-1a9a-4283-a242-df2c129c496dProduct name320170717

Products#

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

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

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
70924-00270924-002-01, 70924-002-02, 70924-002-03, 70924-002-04, 70924-002-05, 70924-002-06, 70924-002-07, 70924-002-09, 70924-002-10, 70924-002-11, 70924-002-12, 70924-002-13, 70924-002-14, 70924-002-15, 70924-002-16, 70924-002-17, 70924-002-19, 70924-002-18

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
NameUNIIKind
WATER059QF0KO0RIACT
PROPYLENE GLYCOL6DC9Q167V3IACT
CAPRYLYL/CAPRYL OLIGOGLUCOSIDEE00JL9G9K0IACT
POLY(LAURYLGLUCOSIDE)-7VB00RDE21RIACT
PHENOXYETHANOLHIE492ZZ3TIACT
BENZOIC ACID8SKN0B0MIMIACT
DEHYDROACETIC ACID2KAG279R6RIACT
BENZALKONIUM CHLORIDEF5UM2KM3W7ACTIB

Source Document#

Source XML

Older Hydrated Versions#

Version, Effective date, Source table
VersionEffective dateSourceHydrated
102025-06-19full-release2026-06-01 01:03:33

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
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Touchpoint Wipes Fragrance Free Sanitizing WipesBENZALKONIUM CHLORIDEInnocore Sales & Marketing Ince805a12d-2bd8-4331-bd81-02c99d057acf2026-07-17WarningsExact identifier
ndc (package): 70924-002-18
ndc (package): 70924-002-03
ndc (package): 70924-002-13
ndc (package): 70924-002-05
ndc (package): 70924-002-06
ndc (package): 70924-002-16
ndc (package): 70924-002-01
ndc (package): 70924-002-10
ndc (package): 70924-002-12
ndc (package): 70924-002-04
ndc (package): 70924-002-14
ndc (package): 70924-002-15
ndc (package): 70924-002-11
ndc (package): 70924-002-07
ndc (package): 70924-002-02
ndc (package): 70924-002-17
ndc (package): 70924-002-19
ndc (package): 70924-002-09
ndc (product): 70924-002
ndc11 (package): 70924000219
ndc11 (package): 70924000207
ndc11 (package): 70924000214
ndc11 (package): 70924000216
ndc11 (package): 70924000217
ndc11 (package): 70924000218
ndc11 (package): 70924000213
ndc11 (package): 70924000206
ndc11 (package): 70924000203
ndc11 (package): 70924000212
ndc11 (package): 70924000215
ndc11 (package): 70924000201
ndc11 (package): 70924000210
ndc11 (package): 70924000205
ndc11 (package): 70924000211
ndc11 (package): 70924000202
ndc11 (package): 70924000209
ndc11 (package): 70924000204
spl id: 56d4aad0-8aba-adbc-e063-6294a90ab235
spl set id: e805a12d-2bd8-4331-bd81-02c99d057acf

Reported adverse events (FAERS/openFDA)#

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