FDA.reportPublic FDA data

Kachi Hand Sanitizer

Manufacturer
J&J SPIRITS
Effective date
2020-08-31
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:26:22

Label at a glance#

ProductKachi Hand Sanitizer
Active ingredientALCOHOL
Label structure8 sections

Dosage and administration

Place enough product on hands to cover all surfaces. Rub hands together until dry. Supervise children under 6 years of age when using this product to avoid swallowing.

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Alcohol 70% v/v

Purpose

OTC - PURPOSE SECTION

Antiseptic

Use

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
in children less than 2 months of age
on open skin wounds
When using this product keep out of eyes, ears, and mouth. In case of contact with eyes, rinse eyes thoroughly with water.
Stop use and ask a doctor if irritation or rash occurs. These may be signs of a serious condition.
Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

  • Place enough product on hands to cover all surfaces. Rub hands together until 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

Product label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image descriptionimage description

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
581662ethanol 70 % Topical GelPSN1
581662ethanol 0.7 ML/ML Topical GelSCD1
581662ethanol 70 % Topical GelSY1
581662ethyl alcohol 70 % Topical GelSY1

DailyMed Product Concepts#

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

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
80219-001-012022-01-28C16284748780-1d6a99b39-6000-a426-e053-dadaa90af4c26b66fd5b-b691-445b-af87-aa6548cac9d0
80219-001-022022-01-28C16284748780-1d6a99b39-6000-a426-e053-dadaa90af4c26b66fd5b-b691-445b-af87-aa6548cac9d0
80219-001-032022-01-28C16284748780-1d6a99b39-6000-a426-e053-dadaa90af4c26b66fd5b-b691-445b-af87-aa6548cac9d0
80219-001-042022-01-28C16284748780-1d6a99b39-6000-a426-e053-dadaa90af4c26b66fd5b-b691-445b-af87-aa6548cac9d0
80219-001-052022-01-28C16284748780-1d6a99b39-6000-a426-e053-dadaa90af4c26b66fd5b-b691-445b-af87-aa6548cac9d0
80219-001-062022-01-28C16284748780-1d6a99b39-6000-a426-e053-dadaa90af4c26b66fd5b-b691-445b-af87-aa6548cac9d0
80219-001-072022-01-28C16284748780-1d6a99b39-6000-a426-e053-dadaa90af4c26b66fd5b-b691-445b-af87-aa6548cac9d0
80219-001-082022-01-28C16284748780-1d6a99b39-6000-a426-e053-dadaa90af4c26b66fd5b-b691-445b-af87-aa6548cac9d0

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
80219-001-01Kachi Hand Sanitizer30 mL in 1 BOTTLE, PLASTICGEL301
80219-001-02Kachi Hand Sanitizer60 mL in 1 BOTTLE, PLASTICGEL601
80219-001-03Kachi Hand Sanitizer120 mL in 1 BOTTLE, PLASTICGEL1201
80219-001-04Kachi Hand Sanitizer236 mL in 1 BOTTLE, PLASTICGEL2361
80219-001-05Kachi Hand Sanitizer473 mL in 1 BOTTLE, PLASTICGEL4731
80219-001-06Kachi Hand Sanitizer946 mL in 1 BOTTLE, PLASTICGEL9461
80219-001-07Kachi Hand Sanitizer1892 mL in 1 BOTTLE, PLASTICGEL18921
80219-001-08Kachi Hand Sanitizer3785 mL in 1 BOTTLE, PLASTICGEL37851

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
80219-001KACHI HAND SANITIZER (ALCOHOL) GEL [J&J SPIRITS]1Legacy NDC, 8 package rows20200901_6b66fd5b-b691-445b-af87-aa6548cac9d0.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
80219-00180219-001-01, 80219-001-02, 80219-001-03, 80219-001-04, 80219-001-05, 80219-001-06, 80219-001-07, 80219-001-08

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 4 matching rows.

Name, UNII, Kind table
NameUNIIKind
WATER059QF0KO0RIACT
GLYCERINPDC6A3C0OXIACT
HYDROGEN PEROXIDEBBX060AN9VIACT
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
ae338cf0-bd5a-4b64-e053-2a95a90ab0c76b66fd5b-b691-445b-af87-aa6548cac9d02020-08-31WarningsExact identifier
spl id: ae338cf0-bd5a-4b64-e053-2a95a90ab0c7
spl set id: 6b66fd5b-b691-445b-af87-aa6548cac9d0

Reported adverse events (FAERS/openFDA)#

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