Instant Wipe

Manufacturer
GM Industrial, Inc.
Effective date
2021-01-14
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
full-release
Hydrated at
2026-05-31 23:36:56

Label at a glance#

ProductInstant Wipe
Active ingredientBENZALKONIUM CHLORIDE
Label structure5 sections

Boxed warning

Drug Facts Benzalkonium chloride 0.1% Antiseptic For hand sanitizing to decrease bacteria on the skin. Recommended for repeated use. For external use only When using this product avoid contact with eyes. In case of eye contact, flush eyes with water. Stop use and ask a doctor if irritation or redness develops, or if condition persists for more than 72 hours. Keep out of reach of children. In case of accidental ing...

Label contents#

Full prescribing information#

BOXED WARNING SECTION

Drug Facts

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium chloride 0.1%

OTC - PURPOSE SECTION

Antiseptic

Uses

INDICATIONS & USAGE SECTION

For hand sanitizing to decrease bacteria on the skin.

Recommended for repeated use.

WARNINGS SECTION

For external use only

OTC - WHEN USING SECTION

When using this product avoid contact with eyes. In case of eye contact, flush eyes with water.

OTC - STOP USE SECTION

Stop use and ask a doctor if irritation or redness develops, or if condition persists for more than 72 hours.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. In case of accidental ingestion, seek medical attention or contact a Poison Control Center immediately.

Directions

DOSAGE & ADMINISTRATION SECTION

Wet hands thoroughly with product. Discard wipe in trash receptacle after use. Do not flush. Rub hands together briskly until dry.

Other information

OTHER SAFETY INFORMATION

Store in a cool dry place below 104 F

INACTIVE INGREDIENT SECTION

Water, C9-11 Pareth-6, Cocamidopropyl PG-dimonium chloride phosphate, Dihydroxyethyl cocamine oxide, Acetamidoethanol, Citric acid.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

90 CT 74146-242-9790 CT 74146-242-9790 CT 74146-242-97

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

225 CT 74146-242-87225 CT 74146-242-87225 CT 74146-242-87

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

90 CT 74146-242-9290 CT 74146-242-92

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

225 CT 74146-242-84 225 CT 74146-242-84225 CT 74146-242-84

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1038856benzalkonium Cl 0.1 % Medicated PadPSN3
1038856benzalkonium chloride 1 MG/ML Medicated PadSCD3
1038856benzalkonium chloride 0.1 % Medicated WipesSY3
1038856benzalkonium chloride 0.1 % Topical SwabSY3

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
74146-242-872022-07-29C16284748780-1e4f33bdf-aeb7-d8a0-e053-dadaa90a6e4eb46585f4-fd2b-0900-e053-2995a90a4a69
74146-242-972022-07-29C16284748780-1e4f33bdf-aeb7-d8a0-e053-dadaa90a6e4eb46585f4-fd2b-0900-e053-2995a90a4a69

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
74146-242-84Instant Wipe810.1 mL in 1 CANISTERCLOTH810.13
74146-242-87Instant Wipe4 in 1 BOXCLOTH43
74146-242-92Instant Wipe647.3 mL in 1 CANISTERCLOTH647.33
74146-242-97Instant Wipe6 in 1 BOXCLOTH63

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
74146-242INSTANT WIPE (BENZALKONIUM CHLORIDE) CLOTH [GM INDUSTRIAL, INC.]3Legacy NDC, 4 package rows20210115_b46585f4-fd2b-0900-e053-2995a90a4a69.zip

Products#

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

DailyMed product names page 1 of 1 · 8 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
74146-24274146-242-92, 74146-242-97, 74146-242-84, 74146-242-87

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 6 matching rows.

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
b8dd1968-dac3-94a2-e053-2995a90aae1eb46585f4-fd2b-0900-e053-2995a90a4a692021-01-14Boxed warning, WarningsExact identifier
spl id: b8dd1968-dac3-94a2-e053-2995a90aae1e
spl set id: b46585f4-fd2b-0900-e053-2995a90a4a69

Reported adverse events (FAERS/openFDA)#

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