DelSan by Genus Lifesciences Inc. DelSan™

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- alcohol gel 
Genus Lifesciences Inc.

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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DelSan™

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.

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

aminomethyl propanol1, carbomer1, diisopropyl adipate, fragrance, glycerin, polyethylene glycol-6 (and) aminomethyl propanol-acrylates/vinyl isodecanoate crosspolymer1, purified water, tocopheryl acetate, triethanolamine1

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 - 237 mL Bottle Label

DelSan™
with Vitamin E

ADVANCED
HAND
SANITIZER

KILLS 99%
OF GERMS!*

MADE IN
USA

8 fl oz / 237 mL

DELSAN 
alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 64950-008
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)
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)
diisopropyl adipate (UNII: P7E6YFV72X)
glycerin (UNII: PDC6A3C0OX)
WATER (UNII: 059QF0KO0R)
RAPIDGEL EZ1 (UNII: 33JH4A7R2K)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
TROLAMINE (UNII: 9O3K93S3TK)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 64950-008-02	59 mL in 1 BOTTLE; Type 0: Not a Combination Product	06/01/2020	12/31/2022
2	NDC: 64950-008-08	237 mL in 1 BOTTLE; Type 0: Not a Combination Product	06/01/2020	12/31/2022

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC MONOGRAPH NOT FINAL	part333A	06/01/2020	12/31/2022

Labeler - Genus Lifesciences Inc. (113290444)

Revised: 12/2022

Document Id: 33e28bfd-76db-4363-a545-3dcc772f8d7c

34390-5

Set id: c6674c5e-1156-4946-ac38-602028f97400

Version: 2

Effective Time: 20221220