ONID Wipe

Manufacturer
ONID Technology Corp | Diamond Wipes International
Effective date
2017-06-28
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 22:51:45

Label at a glance#

ProductONID Wipe
Active ingredientALCOHOL
Label structure7 sections

Indications and uses

For hand washing to decrease bacteria on the skin Reccomended for repeated use

Dosage and administration

open packet remove and unfold wipe wipe hands throughly for approximately 15 seconds do not flush

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 75%

Purpose

OTC - PURPOSE SECTION

Antiseptic

Uses

INDICATIONS & USAGE SECTION

  • For hand washing to decrease bacteria on the skin
  • Reccomended for repeated use

Directions

DOSAGE & ADMINISTRATION SECTION

  • open packet
  • remove and unfold wipe
  • wipe hands throughly for approximately 15 seconds
  • do not flush

Keep Out of Reach of Children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swollowed get medical help or contact Poision Control Center imediately.

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Taiwan Hinoki oil, titanium dioxide, water

Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image descriptionimage description

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1307051ethanol 75 % Medicated PadPSN1
1307051ethanol 0.75 ML/ML Medicated PadSCD1
1307051ethanol 75 % Hand Sanitizer WipesSY1
1307051ethyl alcohol 75 % Topical ClothSY1

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
71441-180-10ONID Wipe.82 mL in 1 PACKETSWAB.821

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
71441-180ONID WIPE (ETHANOL) SWAB [ONID TECHNOLOGY CORP]1Current NDC, Legacy NDC, 1 package rows20170628_83d8b8b6-6257-4553-9441-901bb02c3d60.zip

Products#

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

DailyMed product names page 1 of 1 · 6 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
71441-18071441-180-10

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 4 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
ONID WipeETHANOLONID Technology Corp83d8b8b6-6257-4553-9441-901bb02c3d602017-06-28Exact identifier
ndc (package): 71441-180-10
ndc (product): 71441-180
ndc11 (package): 71441018010
spl id: 4ad98338-8e8d-402c-b5de-b0a8dfba52b0
spl set id: 83d8b8b6-6257-4553-9441-901bb02c3d60

Reported adverse events (FAERS/openFDA)#

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