SANUGEL HAND SANITIZER- isopropyl alcohol gel

Sanugel Hand Sanitizer by

Drug Labeling and Warnings

Sanugel Hand Sanitizer by is a Otc medication manufactured, distributed, or labeled by Dynamic Laboratories, Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug Facts

Active Ingredient(s)

Isopropyl alcohol 75% v/v

Purpose

Antiseptic

Use(s)

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

Warnings

For external use only. Flammable. Keep away from heat or flame.

Do not use

• on 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 thoroughly with water.

Stop use and ask a doctor if irritation or rash occurs. 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 on hands to cover all surfaces. Rub hands together until dry.
▪ Supervise children under 6 years of age when using this product to avoid swallowing.

Other Information

• Store between 15-30°C (59-86°F).
• Avoid freezing and heat above 40°C (104°F)

Inactive Ingredients

glycerin, hydrogen peroxide, purified water USP

SPL UNCLASSIFIED SECTION

Kills most germs that cause illness

Packaging

INGREDIENTS AND APPEARANCE

SANUGEL HAND SANITIZER 
isopropyl alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 74654-171
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	75 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
GLYCERIN (UNII: PDC6A3C0OX)
WATER (UNII: 059QF0KO0R)
HYDROGEN PEROXIDE (UNII: BBX060AN9V)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 74654-171-08	236.6 mL in 1 BOTTLE; Type 0: Not a Combination Product	04/06/2020
2	NDC: 74654-171-04	118.3 mL in 1 BOTTLE; Type 0: Not a Combination Product	04/06/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	04/06/2020

Labeler - Dynamic Laboratories, Inc. (963542493)

Establishment
Name	Address	ID/FEI	Business Operations
Dynamic Laboratories, Inc.		963542493	manufacture(74654-171)