FDA.reportPublic FDA data

All Day Antiseptic Cleansing Wipe

Manufacturer
General Resources LLC
Effective date
2020-10-26
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-01 23:09:53

Label at a glance#

ProductAll Day Antiseptic Cleansing Wipe
Active ingredientBENZALKONIUM CHLORIDE
Label structure14 sections

Storage and handling

Other information Store above 0°C (32°F)

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

Drug Facts

OTC - ACTIVE INGREDIENT SECTION

Active ingredient

Benzalkonium Chloride 0.13%

OTC - PURPOSE SECTION

Purpose

Antiseptic

INDICATIONS & USAGE SECTION

Uses

hand sanitizing to help reduce bacteria on the skin

WARNINGS SECTION

Warnings

For external use only

OTC - WHEN USING SECTION

When using this product avoid contact with the eyes. In case of contact, rinse eyes thoroughly with water.

OTC - STOP USE SECTION

​Stop use and ask a doctor if irritation or redness develops or lasts more than 72 hours

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center immediately.

DOSAGE & ADMINISTRATION SECTION

Directions

  • tear open packet, unfold, and use as a washcloth
  • wipe hands thoroughly with cloth and allow to dry

STORAGE AND HANDLING SECTION

Other information

Store above 0°C (32°F)

INACTIVE INGREDIENT SECTION

Inactive ingredients

purified water

OTC - QUESTIONS SECTION

Questions?Call 1-605-646-4060

SPL UNCLASSIFIED SECTION

* Patented formula effectively eliminates 99.99% of harmful germs, bacteria and viruses in as little as 15 seconds; long term protection for up to 24 hours.

Distributed by: General Resources

1430 Haines Avenue, Ste. 108-156

Rapid City, SD 57701

www.alldayprotect.com

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

ALLDAY

ANTISEPTIC CLEANSING WIPE

KILLS 99.99% OF TESTED GERMS*

SAFE FOR ALL AGES

HYPOALLERGENIC

ALCOHOL FREE

1 pre-moistened wipe (7.5 x 8 in / 19 x 20 cm)

AllDay WipeAllDay Wipe

Products#

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

DailyMed product names page 1 of 1 · 4 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
70481-00270481-002-03

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 2 matching rows.

Name, UNII, Kind table
NameUNIIKind
WATER059QF0KO0RIACT
BENZALKONIUM CHLORIDEF5UM2KM3W7ACTIB

Source Document#

Source XML

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
b299196f-fda3-7c27-e053-2a95a90aff9899742a62-74cb-9c25-e053-2a95a90a41ca2020-10-26WarningsExact identifier
spl id: b299196f-fda3-7c27-e053-2a95a90aff98
spl set id: 99742a62-74cb-9c25-e053-2a95a90a41ca

Reported adverse events (FAERS/openFDA)#

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