Latalia alcohol disinfectant wipes

Manufacturer
INTERNATIONAL CONSUMER PRODUCTS (PVT.) LTD
Effective date
2026-02-03
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-06-01 01:36:49

Label at a glance#

ProductLatalia alcohol disinfectant wipes
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

Sanitizing wipe 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 children less than 2 months of age.
  • on open skin wounds
  • Do not re-use wipes

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.

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 )
  • use fresh wipe if your wipe becomes solid or dry
  • Make sure to wet surface completely
  • Allow surface to dry before use

Inactive ingredients

INACTIVE INGREDIENT SECTION

Glycerin, Hydrogen peroxide, Purified Water USP.

Product label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image descriptionimage descriptionimage descriptionimage description

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
2361646ethanol 80 % Medicated PadPSN2
2361646ethanol 0.8 ML/ML Medicated PadSCD2
2361646ethanol 80 % Medicated WipesSY2
2361646ethyl alcohol 80 % Topical ClothSY2

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
Data codeQR Codewww.latalia.usImage_200.jpg, Image_300.jpg

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
5eb9f24b-9328-475e-af0a-18021935eb6aProduct name120180220

FDA-Initiated Inactive NDC Indexing#

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
80016-006-00Latalia alcohol disinfectant wipes200 in 1 BOTTLECLOTH2002
80016-006-00Latalia alcohol disinfectant wipes2.25 mL in 1 PATCHCLOTH2.252
80016-006-01Latalia alcohol disinfectant wipes300 in 1 BOTTLECLOTH3002
80016-006-01Latalia alcohol disinfectant wipes2.25 mL in 1 PATCHCLOTH2.252

Products#

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

DailyMed product names page 1 of 1 · 6 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
80016-00680016-006-00, 80016-006-01

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 alcohol disinfectant wipesETHYL ALCOHOLINTERNATIONAL CONSUMER PRODUCTS (PVT.) LTD4ef3c800-1754-4d9c-81d6-5309db7b04cf2026-02-03WarningsExact identifier
ndc (package): 80016-006-01
ndc (package): 80016-006-00
ndc (product): 80016-006
ndc11 (package): 80016000600
ndc11 (package): 80016000601
spl id: 49ef77ea-ff85-904f-e063-6294a90a1d15
spl set id: 4ef3c800-1754-4d9c-81d6-5309db7b04cf

Reported adverse events (FAERS/openFDA)#

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