FDA.reportPublic FDA data

Astral Organica Hand Sanitizer

Manufacturer
Kabana Skin Care
Effective date
2024-10-23
Label type
HUMAN OTC DRUG LABEL
Version
5
Source
legacy-cache
Hydrated at
2026-08-01 20:51:22

Label at a glance#

ProductAstral Organica Hand Sanitizer
Active ingredientALCOHOL
Label structure1 sections

Label contents#

Full prescribing information#

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Package Insert - label is too small for Drug Facts Table AstralOrganica Hand SanitizerAstralOrganica Hand Sanitizer

Astral Organica Hand Sanitizer Label - note QR Code referencing Drug Facts for easy access via smart device.

AstralOrganica HS LabelAstralOrganica HS Label

ACTIVE INGREDIENT

OTC - ACTIVE INGREDIENT SECTION

ETHYL ALCOHOL 70% V/V

PURPOSE

OTC - PURPOSE SECTION

ANTIMICROBIAL

OTC - WHEN USING SECTION

WHEN USING THIS PRODUCT, DO NOT USE IN OR NEAR THE EYES. IN CASE OF CONTACT, RINSE EYES THOROUGHLY WITH WATER.

OTC - STOP USE SECTION

DISCONTINUE USE IF IRRITATION OR REDNESS DEVELOPS.

IF CONDITION PERSISTS FOR MORE THAN 72 HOURS, CONSULT A DOCTOR.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

KEEP OUT OF REACH OF CHILDREN. IF SWALLOWED, GET MEDICAL HELP OR CONTACT A POISON CENTER RIGHT AWAY.

USE

INDICATIONS & USAGE SECTION

HAND SANITIZER TO HELP REDUCE PATHOGENS ON THE SKIN

WARNINGS

WARNINGS SECTION

FLAMMABLE. KEEP AWAY FROM FIRE OR FLAME.

THIS PRODUCT IS INTENDED FOR EXTERNAL USE ONLY.

DIRECTIONS

DOSAGE & ADMINISTRATION SECTION

  • PLACE ENOUGH PRODUCT IN YOUR PALM TO THOROUGHLY COVER YOUR HANDS
  • RUB HANDS TOGETHER BRISKLY UNITL DRY
  • CHILDREN UNDER 6 YEARS OF AGE SHOULD BE SUPERVISED WHEN USING THIS PRODUCT

OTHER INFORMATION

OTHER SAFETY INFORMATION

  • STORE BELOW 110oF (44oC)
  • MAY DISCOLOR CERTAIN FABRICS OR SURFACES

INACTIVE INGREDIENTS

INACTIVE INGREDIENT SECTION

WATER (AQUA), HYDROXYETHYLCELLULOSE

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
73369-001073369-0010-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 3 matching rows.

Name, UNII, Kind table
NameUNIIKind
ALCOHOL3K9958V90MACTIB
HYDROXYETHYL CELLULOSE, UNSPECIFIEDT4V6TWG28DIACT
WATER059QF0KO0RIACT

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
31cf4bb0-4b4a-771a-e063-6394a90ab505abea4b76-cafe-799e-e053-2995a90adc3b2025-04-02WarningsExact identifier
spl set id: abea4b76-cafe-799e-e053-2995a90adc3b

Reported adverse events (FAERS/openFDA)#

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