FDA.reportPublic FDA data

Trip Wipes

Manufacturer
DETROIT WICK | Precare Corp
Effective date
2022-12-13
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:52:31

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 between 15°-30°C (59°F - 86°F). Avoid freezing and excessive heat above 40°C (104°F)

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 between 15°-30°C (59°F - 86°F).

Avoid freezing and excessive heat above 40°C (104°F)

Inactive ingredients

INACTIVE INGREDIENT SECTION

Purified Water, Aloe Barbadensis Leaf Extract, Citric Acid, Fragrance, Phenoxyethanol, Polysorbate 20, Potassium Sorbate, Sodium Benzoate, Vitamin E

Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

TRIP WIPES 10CTTRIP WIPES 10CT

73030-025-01

ANTI-BACTERIAL WIPES

SMELLS AMAZING • SOFTENS HANDS

10 BIG WIPES

KILLS 99.9% OF GERMS

DO NOT FLUSH

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1038558benzalkonium chloride 0.13 % Medicated PadPSN1
1038558benzalkonium chloride 1.3 MG/ML Medicated PadSCD1
1038558benzalkonium chloride 0.13 % Topical ClothSY1
1038558benzalkonium chloride 0.13 % Topical SwabSY1
1038558benzalkonium chloride 0.13 GM per 100 GM Topical PadSY1
1038558benzalkonium chloride 0.13 GM per 100 GM Topical SwabSY1
1038558benzalkonium chloride 1 ML per 750 ML Topical SwabSY1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
73030-025-012024-01-30C16284748780-11030e365-15e9-111a-e063-dadaa90a10e2Drug Facts

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
73030-025-01Trip Wipes1 g in 1 PACKETCLOTH11
73030-025-01Trip Wipes10 in 1 BOXCLOTH101

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
73030-025TRIP WIPES (BENZALKONIUM CHLORIDE) CLOTH [DETROIT WICK]1Legacy NDC, 2 package rows20221217_efbb369f-faf3-b98f-e053-2995a90a22cd.zip

Products#

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

DailyMed product names page 1 of 1 · 11 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
73030-02573030-025-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 9 matching rows.

Name, UNII, Kind table
NameUNIIKind
PHENOXYETHANOLHIE492ZZ3TIACT
POTASSIUM SORBATE1VPU26JZZ4IACT
SODIUM BENZOATEOJ245FE5EUIACT
POLYSORBATE 207T1F30V5YHIACT
BENZALKONIUM CHLORIDEF5UM2KM3W7ACTIB
CITRIC ACID MONOHYDRATE2968PHW8QPIACT
.ALPHA.-TOCOPHEROLH4N855PNZ1IACT
WATER059QF0KO0RIACT
ALOE VERA LEAFZY81Z83H0XIACT

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
efbb3cbd-18a4-c224-e053-2995a90ac335efbb369f-faf3-b98f-e053-2995a90a22cd2022-12-13WarningsExact identifier
spl id: efbb3cbd-18a4-c224-e053-2995a90ac335
spl set id: efbb369f-faf3-b98f-e053-2995a90a22cd

Reported adverse events (FAERS/openFDA)#

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