FDA.reportPublic FDA data

go wipes

Manufacturer
American Hygiene Industries
Effective date
2010-07-08
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 22:25:26

Label at a glance#

Productgo wipes
Active ingredientbenzalkonium chloride
Label structure5 sections

Label contents#

Full prescribing information#

DESCRIPTION SECTION


Uses

For hand washing to decrease bacteria on skin

OTC - ACTIVE INGREDIENT SECTION

Active Ingredient                     Purpose
Benzalkonium Chloride 0.13%   Antiseptic

WARNINGS SECTION


Warnings

  • For external use only
  • Do not use if you are allergic to any of the ingredients
  • When using this product do not get into eyes. If contact occurs, rinse thoroughly with water.
  • Discontinue use if irritation or redness develops if condition persists for more than 72 hours consult a physician
  • Keep out of reach of children unless under adult supervision. If swallowed get medical help or contact a Poison Control Center immediately.

INDICATIONS & USAGE SECTION

Directions for use

Thoroughly wipe hands or face with wipe. Discard in trash receptacle; do not flush. Be sure to reseal label complete to retain moisture.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

label
label

American Hygiene

go anywhere wipes

Antibacterial skin sanitizing wipes

kills 99.99% germs

safe on hands and face

non sticky formula with vitamin e and aloe

thick strong 5" x 8" wipe

Join the movement

10 wet wipes

resealable pull tab


DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1038856benzalkonium Cl 0.1 % Medicated PadPSN1
1038856benzalkonium chloride 1 MG/ML Medicated PadSCD1
1038856benzalkonium chloride 0.1 % Medicated WipesSY1
1038856benzalkonium chloride 0.1 % Topical SwabSY1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
50183-112-112019-10-21C16284748780-1956f9ecf-bccd-621f-e053-dbdaa90a74adgo wipes

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
50183-112-11go wipes3.48 g in 1 PACKETCLOTH3.481
50183-112-11go wipes10 in 1 POUCHCLOTH101

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
50183-112GO WIPES (BENZALKONIUM CHLORIDE) CLOTH [AMERICAN HYGIENE INDUSTRIES]1Legacy NDC, 2 package rows20100804_fb4c5871-8a88-4451-8cf9-5b60e6c66e25.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
benzalkonium chlorideACTIVE INGREDIENTF5UM2KM3W71
benzalkoniumACTIVE MOIETY7N6JUD5X6Y1

Products#

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

DailyMed product names page 1 of 1 · 3 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
50183-11250183-112-11

Ingredients#

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

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

Name, UNII, Kind table
NameUNIIKind
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
c42571fb-3f0e-4328-92c7-759ff5140b55fb4c5871-8a88-4451-8cf9-5b60e6c66e252010-07-08WarningsExact identifier
spl id: c42571fb-3f0e-4328-92c7-759ff5140b55
spl set id: fb4c5871-8a88-4451-8cf9-5b60e6c66e25

Reported adverse events (FAERS/openFDA)#

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