FDA.reportPublic FDA data

Lilkoi Hand Sanitizing Wipes

Manufacturer
D-Time Limited Liability Company
Effective date
2021-11-02
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-05-31 23:44:42

Label at a glance#

ProductLilkoi Hand Sanitizing Wipes
Active ingredientALCOHOL
Label structure9 sections

Indications and uses

For personal hand hygiene to help prevent the spread of bacteria.

Dosage and administration

Adults and children over 2 years. For occasional and personal domestic use. Supervise children when they use this product. Rub thoroughly into hands for at least 30 seconds. Allow to dry.

Storage and handling

Store at 68-70  0 F (20-25 0 C) May discolor certain fabrics or surfaces.

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Alcohol 80% v/v. 

Purpose

OTC - PURPOSE SECTION

Antiseptic skin cleanser

Uses

INDICATIONS & USAGE SECTION

For personal hand hygiene to help prevent the spread of bacteria.

Warnings

WARNINGS SECTION

For external use only. 
When using this product avoid contact with eyes. If contact occurs, rinse thoroughly with water.
Stop use and consult a healthcare professional if irritation develops.

Flammability warning: Flammable. Keep away from open flame and sources of heat.

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

Adults and children over 2 years. For occasional and personal domestic use. Supervise children when they use this product. Rub thoroughly into hands for at least 30 seconds. Allow to dry.

Other information

STORAGE AND HANDLING SECTION

  • Store at 68-70  0F (20-25 0C)
  • May discolor certain fabrics or surfaces.

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water, Isopropyl alcohol, Glycerin, Hyaluronic Acid, Bergamot leaf oil, Lavender Flower Oil, Hydrogen Peroxide, Centella Asiatica Extract, Sodium pyruvate

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Label 2Label 2Label 2Label 2

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

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
75306-010-012023-01-30C16284748780-1f386c649-a671-0266-e053-dadaa90a7c1af9210b9b-bfee-43b4-a1ae-4fe9669d3de6
75306-010-022023-01-30C16284748780-1f386c649-a671-0266-e053-dadaa90a7c1af9210b9b-bfee-43b4-a1ae-4fe9669d3de6
75306-010-032023-01-30C16284748780-1f386c649-a671-0266-e053-dadaa90a7c1af9210b9b-bfee-43b4-a1ae-4fe9669d3de6
75306-010-042023-01-30C16284748780-1f386c649-a671-0266-e053-dadaa90a7c1af9210b9b-bfee-43b4-a1ae-4fe9669d3de6
75306-010-052023-01-30C16284748780-1f386c649-a671-0266-e053-dadaa90a7c1af9210b9b-bfee-43b4-a1ae-4fe9669d3de6
75306-010-062023-01-30C16284748780-1f386c649-a671-0266-e053-dadaa90a7c1af9210b9b-bfee-43b4-a1ae-4fe9669d3de6
75306-010-072023-01-30C16284748780-1f386c649-a671-0266-e053-dadaa90a7c1af9210b9b-bfee-43b4-a1ae-4fe9669d3de6
75306-010-082023-01-30C16284748780-1f386c649-a671-0266-e053-dadaa90a7c1af9210b9b-bfee-43b4-a1ae-4fe9669d3de6
75306-010-092023-01-30C16284748780-1f386c649-a671-0266-e053-dadaa90a7c1af9210b9b-bfee-43b4-a1ae-4fe9669d3de6

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
75306-010-01Lilkoi Hand Sanitizing Wipes1 in 1 POUCHCLOTH12
75306-010-01Lilkoi Hand Sanitizing Wipes2 mL in 1 NOT APPLICABLECLOTH22
75306-010-02Lilkoi Hand Sanitizing Wipes2 mL in 1 NOT APPLICABLECLOTH22
75306-010-02Lilkoi Hand Sanitizing Wipes10 in 1 POUCHCLOTH102
75306-010-03Lilkoi Hand Sanitizing Wipes2 mL in 1 NOT APPLICABLECLOTH22
75306-010-03Lilkoi Hand Sanitizing Wipes20 in 1 POUCHCLOTH202
75306-010-04Lilkoi Hand Sanitizing Wipes2 mL in 1 NOT APPLICABLECLOTH22
75306-010-04Lilkoi Hand Sanitizing Wipes50 in 1 POUCHCLOTH502
75306-010-05Lilkoi Hand Sanitizing Wipes100 in 1 POUCHCLOTH1002
75306-010-05Lilkoi Hand Sanitizing Wipes2 mL in 1 NOT APPLICABLECLOTH22
75306-010-06Lilkoi Hand Sanitizing Wipes250 in 1 POUCHCLOTH2502
75306-010-06Lilkoi Hand Sanitizing Wipes2 mL in 1 NOT APPLICABLECLOTH22
75306-010-07Lilkoi Hand Sanitizing Wipes2 mL in 1 NOT APPLICABLECLOTH22
75306-010-07Lilkoi Hand Sanitizing Wipes50 in 1 CONTAINERCLOTH502
75306-010-08Lilkoi Hand Sanitizing Wipes100 in 1 CONTAINERCLOTH1002
75306-010-08Lilkoi Hand Sanitizing Wipes2 mL in 1 NOT APPLICABLECLOTH22
75306-010-09Lilkoi Hand Sanitizing Wipes250 in 1 CONTAINERCLOTH2502
75306-010-09Lilkoi Hand Sanitizing Wipes2 mL in 1 NOT APPLICABLECLOTH22

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
75306-010LILKOI HAND SANITIZING WIPES (ALCOHOL) CLOTH [D-TIME LIMITED LIABILITY COMPANY]2Legacy NDC, 18 package rows20211103_f9210b9b-bfee-43b4-a1ae-4fe9669d3de6.zip

Products#

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

DailyMed product names page 1 of 1 · 11 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
75306-01075306-010-01, 75306-010-02, 75306-010-03, 75306-010-04, 75306-010-05, 75306-010-06, 75306-010-07, 75306-010-08, 75306-010-09

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 10 matching rows.

Name, UNII, Kind table
NameUNIIKind
WATER059QF0KO0RIACT
ISOPROPYL ALCOHOLND2M416302IACT
GLYCERINPDC6A3C0OXIACT
HYALURONIC ACIDS270N0TRQYIACT
BERGAMOT OIL39W1PKE3JIIACT
LAVENDER OILZBP1YXW0H8IACT
HYDROGEN PEROXIDEBBX060AN9VIACT
CENTELLA ASIATICA7M867G6T1UIACT
SODIUM PYRUVATEPOD38AIF08IACT
ALCOHOL3K9958V90MACTIB

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
cfd12826-b83d-0898-e053-2995a90a48f7f9210b9b-bfee-43b4-a1ae-4fe9669d3de62021-11-02WarningsExact identifier
spl id: cfd12826-b83d-0898-e053-2995a90a48f7
spl set id: f9210b9b-bfee-43b4-a1ae-4fe9669d3de6

Reported adverse events (FAERS/openFDA)#

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