Disinfectant Wipes

Manufacturer
GUANGZHOU DICALLO CO.,LTD
Effective date
2020-10-30
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-05-31 23:32:40

Label at a glance#

ProductDisinfectant Wipes
Active ingredientALCOHOL
Label structure7 sections

Label contents#

Full prescribing information#

DOSAGE & ADMINISTRATION SECTION

Use one wipe per object to avoid cross contamination.

Seal after each use.

Avoid direct contact with eyes, if so flush with plenty if water for 15 minutes immediately.

Supervise children under 6 years of age when using this product to avoid swallowing.

INACTIVE INGREDIENT SECTION

Gylcerin, Hydrogen Proxide, Ro Pure Water

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 75%…………Antimicriobial

WARNINGS SECTION

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

OTC - ASK DOCTOR SECTION

Stop the use and ask a doctor if irritation or rash occurs. These may signs if serious conditions.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

OTC - DO NOT USE SECTION

Do not use

  • in child less than 2 months of age.
  • on open skin wounds.

OTC - WHEN USING SECTION

When using this product, keep out od eyes, ears, and mouth. In case of contact with eyes, rinse thoroughly with water.

INDICATIONS & USAGE SECTION

Helps reduce bacteria on the skin.

OTC - PURPOSE SECTION

Helpa reduce bacrteria on the skin.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

PackagePackage

FDA-Initiated Inactive NDC Indexing#

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
79600-001-01Disinfectant Wipes50 in 1 PACKAGESWAB502
79600-001-02Disinfectant Wipes60 in 1 BOTTLESWAB602
79600-001-03Disinfectant Wipes260 in 1 CANISTERSWAB2602

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
79600-001DISINFECTANT WIPES SWAB [GUANGZHOU DICALLO CO.,LTD]2Legacy NDC, 3 package rows20201031_aa99e7cf-7b15-0e7b-e053-2995a90a98bc.zip

Products#

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

DailyMed product names page 1 of 1 · 5 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
79600-00179600-001-01, 79600-001-02, 79600-001-03

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
b2e093f8-4fb4-7fd4-e053-2995a90a67afaa99e7cf-7b15-0e7b-e053-2995a90a98bc2020-10-30WarningsExact identifier
spl id: b2e093f8-4fb4-7fd4-e053-2995a90a67af
spl set id: aa99e7cf-7b15-0e7b-e053-2995a90a98bc

Reported adverse events (FAERS/openFDA)#

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