DelSan™ Hand Sanitizer with Vitamin E

DelSan by

Drug Labeling and Warnings

DelSan by is a Otc medication manufactured, distributed, or labeled by Genus Lifesciences Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

DELSAN  HAND SANITIZER WITH VITAMIN E- alcohol gel 
Genus Lifesciences Inc.

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DelSan™
Hand Sanitizer with Vitamin E

Drug Facts

Active ingredient

‡ Ethyl alcohol 70% v/v

Purpose

Antiseptic

Use

• Hand Sanitizer to help reduce bacteria that potentially can cause disease

Warnings

Flammable. Keep away from heat or flame

For external use only - hands

Do not use

• in children less than 2 months of age
• on open skin wounds

When using this product 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 skin irritation or rash appears and lasts. These may be signs of a serious condition.

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Directions

• Place 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 this product.

Other information

• Store between 15 - 30°C (59 - 86°F)
• Avoid freezing and excessive heat above 40°C (104°F)
• May discolor certain fabrics
• May be harmful to wood finishes and plastics

Inactive ingredients

Acrylates/C10-30 Alkyl Acrylate Crosspolymer 1, Aminomethyl propanol, Betaine 1, Diisopropyl adipate, Aloe Barbadenis extract, Fragrance, Glycerin, Purified water, Vitamin E acetate

1 contains one or more of these ingredients

Questions?

Call Pharm-Olam at 1-866-511-6754

Distributed by: Genus Lifesciences Inc. Allentown, PA 18102

PRINCIPAL DISPLAY PANEL - 59 mL Bottle Label

DelSan™
with Vitamin E

KILLS 99.9%
OF GERMS!*

ALOE
HAND
SANITIZER

‡70%
MOISTURIZING

2 fl oz / 59 mL

DELSAN   HAND SANITIZER WITH VITAMIN E
alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 64950-020
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (alcohol - UNII:3K9958V90M)	ALCOHOL	70 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
AMINOMETHYLPROPANOL (UNII: LU49E6626Q)
ALOE VERA FLOWER (UNII: 575DY8C1ER)
betaine (UNII: 3SCV180C9W)
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)
diisopropyl adipate (UNII: P7E6YFV72X)
glycerin (UNII: PDC6A3C0OX)
water (UNII: 059QF0KO0R)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 64950-020-02	59 mL in 1 BOTTLE; Type 0: Not a Combination Product	10/29/2020	12/31/2022
2	NDC: 64950-020-08	237 mL in 1 BOTTLE; Type 0: Not a Combination Product	10/29/2020	12/31/2022

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph drug	M004	10/29/2020	12/31/2022

Labeler - Genus Lifesciences Inc. (113290444)

Revised: 12/2022

Document Id: 6cfaeaf1-d209-4f87-a526-3c83cd9f4b0a

34390-5

Set id: 15b67f61-be1c-4abc-9082-bfa48576a9ca

Version: 2

Effective Time: 20221220