IS Clinical Hand Sanitizing 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, V Manufacturing & Logistics, Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

IS CLINICAL HAND SANITIZING GEL- ethyl alcohol gel 
SCIENCE OF SKINCARE LLC

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

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IS Clinical Hand Sanitizing Gel

Active Ingredient

Ethyl Alcohol 62% v/v

Purpose

Antiseptic

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

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

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

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

Uses to help reduce bacteria on the skin.

Directions

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

Other information

• Do not store above 104°F (40°C).

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.

IS CLINICAL HAND SANITIZING GEL 
ethyl alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 69219-106
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: 69219-106-16	480 mL in 1 BOTTLE; Type 0: Not a Combination Product	05/27/2020	05/27/2022

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	05/27/2020	05/27/2022

Labeler - SCIENCE OF SKINCARE LLC (006251958)

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

Revised: 5/2020

Document Id: a6aae931-2cab-9f7d-e053-2995a90ad615

34390-5

Set id: a6aaeab4-c0a1-9218-e053-2995a90a373c

Version: 1

Effective Time: 20200527