KORA Daily Safe 70

Manufacturer
Kora Holdings LLC | Sellus
Effective date
2020-12-15
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-05-31 23:35:38

Label at a glance#

ProductKORA Daily Safe 70
Active ingredientALCOHOL
Label structure12 sections

Dosage and administration

Put enough product in your palm to cover hands and rub hands together briskly until dry. Children under 6 years of age should be supervised when using.

Storage and handling

Store below 110°F (43°C)

Label contents#

Full prescribing information#

Active Ingredient(s)

OTC - ACTIVE INGREDIENT SECTION

Alcohol 70% v/v. Purpose: Antiseptic

Purpose

OTC - PURPOSE SECTION

Antiseptic. hand Sanitizer

Use

INDICATIONS & USAGE SECTION

For hand sanitizer to reduct microorganisms that potentially can cause diseases. Recommended for repeated use.

Warnings

WARNINGS SECTION

For external use on hands only. Flammable. Keep away from fire or flame.

Do not use

OTC - DO NOT USE SECTION

ir or near the eyes. In case of contact with eyes, rinse eyes thoroughly with water.

OTC - WHEN USING SECTION

When using this product do not use in or near the eyes. In case of contact with eyes, rinse eyes thoroughly with water.

Stop use and ask a doctor if irritation, swelling or redness develops.

Keep out of reach of children. if swallowed, get medical help or contact a Poison Control Center immediately.

OTC - STOP USE SECTION

Stop use and ask a doctor if irritation, swelling or redness develops.

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 immediately.

Directions

DOSAGE & ADMINISTRATION SECTION

Put enough product in your palm to cover hands and rub hands together briskly until dry.

Children under 6 years of age should be supervised when using.

Other information

STORAGE AND HANDLING SECTION

Store below 110°F (43°C)

Inactive ingredients

INACTIVE INGREDIENT SECTION

Ethyl alcohol, Sterile Distilled Water, Carbomer, Triethanolamine, Polyglyceryl-2-triisostearate, Dipropylene glycol, L-Menthol, Sodium Hyaluronate 1%, Lemon fragrance

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

500mL

NDC:75504-170-11

KORA Daily Safe 70KORA Daily Safe 70

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
581662ethanol 70 % Topical GelPSN2
581662ethanol 0.7 ML/ML Topical GelSCD2
581662ethanol 70 % Topical GelSY2
581662ethyl alcohol 70 % Topical GelSY2

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
75504-170-112022-01-28C16284748780-1d6a99b39-b4eb-a426-e053-dadaa90af4c2a442d54a-1dc3-f795-e053-2a95a90ab3c0

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
75504-170-11KORA Daily Safe 70500 mL in 1 BOTTLE, PUMPGEL5002

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
75504-170KORA DAILY SAFE 70 (HAND SANITIZER GEL) GEL [KORA HOLDINGS LLC]2Legacy NDC, 1 package rows20201221_a442d54a-1dc3-f795-e053-2a95a90ab3c0.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
75504-17075504-170-11

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 9 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
b68b6e8a-a198-179d-e053-2a95a90ace87a442d54a-1dc3-f795-e053-2a95a90ab3c02020-12-15WarningsExact identifier
spl id: b68b6e8a-a198-179d-e053-2a95a90ace87
spl set id: a442d54a-1dc3-f795-e053-2a95a90ab3c0

Reported adverse events (FAERS/openFDA)#

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