IS CLINICAL HAND SANITIZING GEL- ethyl alcohol gel

IS Clinical Hand Sanitizing Gel by

Drug Labeling and Warnings

IS Clinical Hand Sanitizing Gel by is a Otc medication manufactured, distributed, or labeled by SCIENCE OF SKINCARE LLC, KDC/ONE SOCAL LABORATORIES, LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Active Ingredient

Ethyl Alcohol 62% v/v

PURPOSE

Purpose

Antiseptic

WARNINGS

• For external use only.
• Flammable, Keep away from fire or flame.

WHEN USING

When using this product avoid contact with eyes. If eye contact occurs, rinse with water.

STOP USE

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

KEEP OUT OF REACH OF CHILDREN

Keep out of reach of children. In case of accidental ingestion, seek medical help or contact a Poison Control Center immediately.

INDICATIONS & USAGE

Uses to help reduce bacteria on the skin.

DOSAGE & ADMINISTRATION

Directions

• Apply enough gel to wet hands and rub together until dry.
• Use 1 to 3 times daily.

STORAGE AND HANDLING

Other information

• Do not store above 104°F (40°C).

INACTIVE INGREDIENT

Inactive ingredients Aloe Barbadensis Leaf Juice, Glycerin, Helianthus Annuus (Sunflower) Seed Oil, Hydroxyethylcellulose, Lonicera Caprifolium (Honeysuckle) Flower Extract, Lonicera Japonica (Honeysuckle) Flower Extract, Rosmarinus Officinalis (Rosemary) Leaf Extract, Water (Aqua). May contain Isopropyl Alcohol.

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

IS CLINICAL HAND SANITIZING GEL 
ethyl alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 69219-105
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	62 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
ALOE VERA LEAF (UNII: ZY81Z83H0X)
HYDROXYETHYL CELLULOSE (100 MPA.S AT 2%) (UNII: R33S7TK2EP)
GLYCERIN (UNII: PDC6A3C0OX)
SUNFLOWER OIL (UNII: 3W1JG795YI)
ROSEMARY (UNII: IJ67X351P9)
LONICERA JAPONICA FLOWER (UNII: 4465L2WS4Y)
ISOPROPYL ALCOHOL (UNII: ND2M416302)
LONICERA CAPRIFOLIUM FLOWER (UNII: 5N1WD9784U)
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 69219-105-04	120 mL in 1 BOTTLE; Type 0: Not a Combination Product	05/06/2020	05/06/2022

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	05/06/2020	05/06/2022

Labeler - SCIENCE OF SKINCARE LLC (006251958)

Registrant - V Manufacturing & Logistics, Inc. (079081508)