FDA.reportPublic FDA data

Trip Wipes

Manufacturer
DETROIT WICK | Precare Corp
Effective date
2024-12-06
Label type
HUMAN OTC DRUG LABEL
Version
7
Source
full-release
Hydrated at
2026-06-01 00:41:39

Label at a glance#

ProductTrip Wipes
Active ingredientBENZALKONIUM CHLORIDE
Label structure8 sections

Indications and uses

For hand sanitizing to decrease bacteria on the skin Recommended for repeated use

Dosage and administration

take wipe and rub thoroughly over all surfaces of both hands. Wet hands thoroughly with wipe rub hands together briskly to dry without wiping dispose of wipe do not flush

Storage and handling

Store in a cool dry place

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium chloride 0.13%

Purpose

OTC - PURPOSE SECTION

Antimicrobial

Uses

INDICATIONS & USAGE SECTION

  • For hand sanitizing to decrease bacteria on the skin
  • Recommended for repeated use

Warnings

WARNINGS SECTION

For external use only

When using this product

OTC - WHEN USING SECTION

avoid contact with eyes. In case of eye contact, flush eyes with water.

Stop use and ask a doctor

OTC - STOP USE SECTION

If irritation or redness develops, or if condition persists for more than 72 hours.

Keep out of reach of children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, get medical help or contact a Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

  • take wipe and rub thoroughly over all surfaces of both hands. Wet hands thoroughly with wipe
  • rub hands together briskly to dry without wiping
  • dispose of wipe
  • do not flush

Other information

STORAGE AND HANDLING SECTION

Store in a cool dry place

Inactive ingredients

INACTIVE INGREDIENT SECTION

Purified Water, Phenoxyethanol, Potassium Sorbate, Sodium Benzoate, Citric Acid, Polysorbate 20, Citrus Aurantium Dulcis Oil, Citrus Grandis Peel Oil, Citrus Aurantium Bergamia Fruit Oil, Elettaria Cardamomum Miniscula Seed, Linolool, Ehylene Brassylate, Citral, Kumquat Base, Galaxolide

Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Artwork 1Artwork 1

NDC 73030-020-02

DO NOT FLUSH

CLEAN IS A WIPE AWAY

TRIP WIPES

CITRUS ANTI-BACTERIAL WIPE

1 INDIVIDUAL WIPE

Artwork 2Artwork 2

NDC 73030-020-01

MADE IN THE USA

ALCOHOL-FREE WIPES FOR ON-THE-GO

For Planes, Trains +

Handshakes

TRAVEL IN PEACE

KILLS 99.9% OF GERMS

SMELLS AMAZING

SOFTENS HANDS

SHARE WITH YOU FRIENDS

30 ANTIBACTERIAL WIPES

CITRUS SCENTED

TRIPWIPES.COM

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1038558benzalkonium chloride 0.13 % Medicated PadPSN7
1038558benzalkonium chloride 1.3 MG/ML Medicated PadSCD7
1038558benzalkonium chloride 0.13 % Topical ClothSY7
1038558benzalkonium chloride 0.13 % Topical SwabSY7
1038558benzalkonium chloride 0.13 GM per 100 GM Topical PadSY7
1038558benzalkonium chloride 0.13 GM per 100 GM Topical SwabSY7
1038558benzalkonium chloride 1 ML per 750 ML Topical SwabSY7

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
73030-020-012026-01-29C16284748780-149896155-bff4-586f-e063-e6dba90add90Drug Facts
73030-020-022026-01-29C16284748780-149896155-bff4-586f-e063-e6dba90add90Drug Facts

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
73030-020-01Trip Wipes30 in 1 BOXSWAB307
73030-020-01Trip Wipes1 g in 1 PACKETSWAB17
73030-020-02Trip Wipes1 g in 1 PACKETSWAB17
73030-020-02Trip Wipes1 in 1 PACKETSWAB17

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
73030-020TRIP WIPES (BENZALKONIUM CHLORIDE) SWAB [DETROIT WICK]7Legacy NDC, 4 package rows20241211_8a78b431-6b38-4ef8-b470-d99665d78948.zip

Products#

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

DailyMed product names page 1 of 1 · 17 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
73030-02073030-020-01, 73030-020-02

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 15 matching rows.

Name, UNII, Kind table
NameUNIIKind
WATER059QF0KO0RIACT
PHENOXYETHANOLHIE492ZZ3TIACT
POTASSIUM SORBATE1VPU26JZZ4IACT
SODIUM BENZOATEOJ245FE5EUIACT
CITRIC ACID MONOHYDRATE2968PHW8QPIACT
POLYSORBATE 207T1F30V5YHIACT
ORANGE OILAKN3KSD11BIACT
CITRUS MAXIMA FRUIT RIND OIL8U3877WD44IACT
BERGAMOT OIL39W1PKE3JIIACT
LINALOOL, (+/-)-D81QY6I88EIACT
ETHYLENE BRASSYLATE9A87HC7RODIACT
CITRALT7EU0O9VPPIACT
CITRUS JAPONICA FRUIT8PS197OFKTIACT
HEXAMETHYLINDANOPYRAN14170060ATIACT
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
28a11cb0-f883-8f70-e063-6294a90aebc88a78b431-6b38-4ef8-b470-d99665d789482024-12-06WarningsExact identifier
spl id: 28a11cb0-f883-8f70-e063-6294a90aebc8
spl set id: 8a78b431-6b38-4ef8-b470-d99665d78948

Reported adverse events (FAERS/openFDA)#

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