Latalia Sanitizing Wipe

Manufacturer
INTERNATIONAL CONSUMER PRODUCTS (PVT.) LTD
Effective date
2024-01-10
Label type
HUMAN OTC DRUG LABEL
Version
6
Source
full-release
Hydrated at
2026-06-01 00:07:03

Label at a glance#

ProductLatalia Sanitizing Wipe
Active ingredientALCOHOL
Label structure7 sections

Dosage and administration

Wipe hands or all surfaces. Allow to dry. Supervise children under 6 years of age when using this product to avoid swallowing.

Label contents#

Full prescribing information#

Active ingredient[s]

OTC - ACTIVE INGREDIENT SECTION

Alcohol 80% v/v

Purpose

OTC - PURPOSE SECTION

Antiseptic & Antibacterial

Use[s]

INDICATIONS & USAGE SECTION

Hand sanitizer to help reduce bacteria that potentially can cause disease. For use when soap and water are not available.

Warnings

WARNINGS SECTION

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

Do not use

OTC - DO NOT USE SECTION

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

When using this product

OTC - WHEN USING SECTION

keep out of eyes, ears, and mouth. In case of contact with eyes, rinse eyes thoroughly with water.

Stop use and ask a doctor

OTC - STOP USE SECTION

if irritation or rash occurs. These may be signs of a serious condition.

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

Directions

DOSAGE & ADMINISTRATION SECTION

  • Wipe hands or all surfaces. Allow to dry.
  • Supervise children under 6 years of age when using this
  • product to avoid swallowing.

Other information

SPL UNCLASSIFIED SECTION

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

Inactive ingredients

INACTIVE INGREDIENT SECTION

Glycerin, Hydrogen peroxide, Purified Water USP.

Package Labeling:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

BoxBox

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
2361646ethanol 80 % Medicated PadPSN6
2361646ethanol 0.8 ML/ML Medicated PadSCD6
2361646ethanol 80 % Medicated WipesSY6
2361646ethyl alcohol 80 % Topical ClothSY6

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
80016-002-002025-08-08C16284748780-13b156c62-27dc-fb37-e063-e6dba90a4e07Latalia Sanitizing Wipe , 80% Alcohol
80016-002-002025-07-29C16284748780-13b156c62-27dc-fb37-e063-e6dba90a4e07Latalia Sanitizing Wipe , 80% Alcohol

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
80016-002-00Latalia Sanitizing Wipe4 mL in 1 PATCHCLOTH46
80016-002-00Latalia Sanitizing Wipe20 in 1 BOXCLOTH206

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
80016-002LATALIA SANITIZING WIPE (ALCOHOL) CLOTH [INTERNATIONAL CONSUMER PRODUCTS (PVT.) LTD]6Current NDC, Legacy NDC, 2 package rows20240112_ae564635-898e-fbf6-e053-2995a90a8119.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
80016-00280016-002-00

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
Latalia Sanitizing WipeALCOHOLINTERNATIONAL CONSUMER PRODUCTS (PVT.) LTDae564635-898e-fbf6-e053-2995a90a81192024-01-10WarningsExact identifier
ndc (package): 80016-002-00
ndc (product): 80016-002
ndc11 (package): 80016000200
spl id: 0e999a13-bfb0-44f0-e063-6394a90a43af
spl set id: ae564635-898e-fbf6-e053-2995a90a8119

Reported adverse events (FAERS/openFDA)#

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