Hestia Clinic Gel Hand Sanitizer

Manufacturer
DANS-K Medical Supplies LLC
Effective date
2020-08-11
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
legacy-cache
Hydrated at
2026-08-01 23:18:20

Label at a glance#

ProductHestia Clinic Gel Hand Sanitizer
Active ingredientALCOHOL
Label structure7 sections

Indications and uses

Hand Sanitizer to help reduce bacteria on the skin that potentially can cause disease. For use when soap and water are not available.

Dosage and administration

· Place enough product on hands to cover all surfaces. Rub hands together briskly until dry. · Place more hand sanitizer into palm, and rub into fingernails to disinfect. · Supervise children under 6 years of age when using this product to avoid swallowing.

Label contents#

Full prescribing information#

Drug Facts

OTC - ACTIVE INGREDIENT SECTION

Active ingredient: Purpose

Ethyl Alcohol 62% m/m…………...………………….Antiseptic

Purpose

OTC - PURPOSE SECTION

Antiseptic

Uses

INDICATIONS & USAGE SECTION

Hand Sanitizer to help reduce bacteria on the skin 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

OTC - DO NOT USE SECTION

· in children less than 2 months of age, without consulting a physician

· on open skin wounds

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.

Stop use and ask a doctor if:

OTC - STOP USE SECTION

· irritation or rash occurs. These may be signs of a serious condition.

· side effects occur. You may report side effects to FDA at 1-800-FDA-1088.

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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 briskly until dry.

· Place more hand sanitizer into palm, and rub into fingernails to disinfect.

· Supervise children under 6 years of age when using this product to avoid swallowing.

Other Information

OTHER SAFETY INFORMATION

Store between 1-30C (34-86F)

Avoid freezing and excessive heat above 40C (104F)

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Alcohol, Water, Carbomer, Triethanolamine, PEG-60 Hydrogenated Castor Oil, Lavandula Angustifolia (Lavender) Oil, Methylparaben, Butylene Glycol, 1, 2-Hexanediol, Glycosaminoglycans, Fragaria Chiloensis (Strawberry) Fruit Extract, Pyrus Malus (Apple) Fruit Extract, Punica Granatum Fruit Extract, Citrullus Vulgaris (Watermelon) Fruit Extract, Solanum Lycopersicum (Tomato) Fruit Extract, Capsicum Annuum Fruit Extract

Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

100 mL NDC 74002-0100

LabelLabel

Products#

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DailyMed product names page 1 of 1 · 17 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
79656-010079656-0100-1
74002-0100

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 16 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
ad165e36-270c-3527-e053-2995a90a6d2aa8cdc5b3-6049-381d-e053-2a95a90a78ac2020-08-11WarningsExact identifier
spl id: ad165e36-270c-3527-e053-2995a90a6d2a
spl set id: a8cdc5b3-6049-381d-e053-2a95a90a78ac

Reported adverse events (FAERS/openFDA)#

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