FDA.reportPublic FDA data

Miracle Wipes for Hand Sanitizing

Manufacturer
Kelly Products, Inc.
Effective date
2021-02-11
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:44:41

Label at a glance#

ProductMiracle Wipes for Hand Sanitizing
Active ingredientBENZALKONIUM CHLORIDE
Label structure12 sections

Dosage and administration

Wet hands thoroughly with product and allow to dry. Children under six years of age should be surprised when using this product.

Storage and handling

Store in a cool, dry place.

Label contents#

Full prescribing information#

Active Ingredient(s)

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium Chloride 0.13%

Purpose

OTC - PURPOSE SECTION

Antiseptic, Hand Sanitizer

Use

INDICATIONS & USAGE SECTION

Hand Sanitizer to help reduce bacteria that potentially can cause disease.

Warnings

WARNINGS SECTION

For external use only. Flammable. Keep away from heat or flame

Do not use

OTC - DO NOT USE SECTION

  • in the eyes

OTC - WHEN USING SECTION

When using this product do not get into eyes. In case of contact with eyes, rinse eyes thoroughly with water.

OTC - STOP USE SECTION

Stop use and ask a doctor if irritation and redness develop. If condition persists for more than 72 hours consult a doctor.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

  • Wet hands thoroughly with product and allow to dry.
  • Children under six years of age should be surprised when using this product.

Other information

STORAGE AND HANDLING SECTION

  • Store in a cool, dry place.

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water, Cocamidopropyl Betaine, Cetrimonium Chloride, Didecyldimonium Chloride, Allantoin, Fragrance, Aloe, Cocamidopropylamine Oxide, Propylene Glycol, Diazolidinyl Urea, Methylparaben, Propylparaben, Triethonalamine, Vitamin E, Citric Acid

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

70 Wet Wipes 1 Ply NDC: 79779-002-7070 Wet Wipes 1 Ply NDC: 79779-002-7070 Wet Wipes 1 Ply NDC: 79779-002-70

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
79779-002-702023-01-30C16284748780-1f386c649-e242-0266-e053-dadaa90a7c1aMiracle Wipe for Hand Sanitizing

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
79779-002-70Miracle Wipes for Hand Sanitizing70 g in 1 CANISTERCLOTH701

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
79779-002MIRACLE WIPES FOR HAND SANITIZING (BENZALKONIUM CHLORIDE) CLOTH [KELLY PRODUCTS, INC.]1Legacy NDC, 1 package rows20211103_bb196842-9d76-08ec-e053-2995a90a5459.zip

Products#

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

DailyMed product names page 1 of 1 · 18 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
79779-00279779-002-70

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 16 matching rows.

Name, UNII, Kind table
NameUNIIKind
DIDECYLDIMONIUM CHLORIDEJXN40O9Y9BIACT
TROLAMINE9O3K93S3TKIACT
ALOEV5VD430YW9IACT
CITRALT7EU0O9VPPIACT
WATER059QF0KO0RIACT
COCAMIDOPROPYLAMINE OXIDEM4SL82J7HKIACT
CETRIMONIUM CHLORIDEUC9PE95IBPIACT
PROPYLENE GLYCOL6DC9Q167V3IACT
DIAZOLIDINYL UREAH5RIZ3MPW4IACT
BENZALKONIUM CHLORIDEF5UM2KM3W7ACTIB
METHYLPARABENA2I8C7HI9TIACT
ANHYDROUS CITRIC ACIDXF417D3PSLIACT
ORANGE TERPENES9J3RG7FX7SIACT
ALPHA-TOCOPHEROLH4N855PNZ1IACT
ALLANTOIN344S277G0ZIACT
COCAMIDOPROPYL BETAINE5OCF3O11KXIACT

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
bb18034d-44fe-71e2-e053-2a95a90a3857bb196842-9d76-08ec-e053-2995a90a54592021-02-11WarningsExact identifier
spl id: bb18034d-44fe-71e2-e053-2a95a90a3857
spl set id: bb196842-9d76-08ec-e053-2995a90a5459

Reported adverse events (FAERS/openFDA)#

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