MedPath

Cart Wipes Clean Sanitizing Wipes

Cart Wipes™ Clean Sanitizing Wipes

Approved
Approval ID

6a8433e8-7b96-44ce-b8e2-c60575898dab

Product Type

HUMAN OTC DRUG LABEL

Effective Date

Jun 18, 2025

Manufacturers
FDA

Carts and Parts INC.

DUNS: 094773645

Products 1

Detailed information about drug products covered under this FDA approval, including NDC codes, dosage forms, ingredients, and administration routes.

BENZALKONIUM CHLORIDE

Product Details

FDA regulatory identification and product classification information

FDA Identifiers
NDC Product Code82402-010
Application NumberM003
Product Classification
M
Marketing Category
C200263
G
Generic Name
BENZALKONIUM CHLORIDE
Product Specifications
Route of AdministrationTOPICAL
Effective DateJune 18, 2025
FDA Product Classification

INGREDIENTS (10)

BENZALKONIUM CHLORIDEActive
Quantity: 0.0019 g in 1 1
Code: F5UM2KM3W7
Classification: ACTIB
WATERInactive
Code: 059QF0KO0R
Classification: IACT
SODIUM LAURYLGLUCOSIDES HYDROXYPROPYLSULFONATEInactive
Code: Z6GFR7R72Y
Classification: IACT
LAURAMINE OXIDEInactive
Code: 4F6FC4MI8W
Classification: IACT
PHENOXYETHANOLInactive
Code: HIE492ZZ3T
Classification: IACT
METHYLCHLOROISOTHIAZOLINONE/METHYLISOTHIAZOLINONE MIXTUREInactive
Code: 15O9QS218W
Classification: IACT
EDETATE SODIUMInactive
Code: MP1J8420LU
Classification: IACT
ALOE VERA LEAFInactive
Code: ZY81Z83H0X
Classification: IACT
.ALPHA.-TOCOPHEROL ACETATEInactive
Code: 9E8X80D2L0
Classification: IACT
PEG-75 LANOLINInactive
Code: 09179OX7TB
Classification: IACT

Drug Labeling Information

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

LOINC: 51945-4Updated: 6/18/2025

PRINCIPAL DISPLAY PANEL - 1200 Wipe Pouch Label

Carts & Parts, Inc.

cartWipes™
CLEAN

AVAILABLE ONLY THROUGH CARTS & PARTS, INC.
1-800-424-2278
WWW.CARTSANDPARTS.COM

SANITIZING WIPES

NOT TO BE USED AS A BABY WIPE

DO NOT FLUSH

PRINCIPAL DISPLAY PANEL - 1200 Wipe Pouch Label

INDICATIONS & USAGE SECTION

LOINC: 34067-9Updated: 6/18/2025

Uses

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

SPL UNCLASSIFIED SECTION

LOINC: 42229-5Updated: 6/18/2025

Drug Facts

OTC - ACTIVE INGREDIENT SECTION

LOINC: 55106-9Updated: 6/18/2025

Active Ingredient

Benzalkonium Chloride 0.13%

OTC - PURPOSE SECTION

LOINC: 55105-1Updated: 6/18/2025

Purpose

Antimicrobial

WARNINGS SECTION

LOINC: 34071-1Updated: 6/18/2025

Warnings

  • 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.

  • Keep out of reach of children.

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

DOSAGE & ADMINISTRATION SECTION

LOINC: 34068-7Updated: 6/18/2025

Directions

Take wipe and rub thoroughly over all surfaces of both hands. Rub hands together briskly to dry. Dispose of wipe.

INACTIVE INGREDIENT SECTION

LOINC: 51727-6Updated: 6/18/2025

Inactive Ingredients

Water, 2-Phenoxyethanol, Alkylpolyglucoside, C8-10, C10-16, Fragrance, Lauramine, N-dimethyl, N-oxide, Tocopherol acetate, Aloe barbadensis leaf juice, PEG-40 Lanolin, Tetrasodium, EDTA, Methylchloroisothiazoline, Methylisothiazoline. Nonwoven disposable cloth.

OTC - QUESTIONS SECTION

LOINC: 53413-1Updated: 6/18/2025

FOR EMERGENCY MEDICAL INFORMATION CALL (914) 683-5800 (M-F DAYTIME)
AT OTHER TIMES CONTACT YOUR LOCAL POISON CONTROL CENTER

FOR SERVICE OR ADDITIONAL INFORMATION CALL 1-800-424-2278

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