Enzysept by HP&C, Ltd. ENZYSEPT- alcohol gel

Enzysept by

Drug Labeling and Warnings

Enzysept by is a Otc medication manufactured, distributed, or labeled by HP&C, Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

SPL UNCLASSIFIED SECTION

Drug Facts

Active ingredient

Ethyl Alcohol 83% w/w

Purpose

Antiseptic

Uses

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 open skin wounds

When using this product avoid contact with face, eyes, and broken skin. If eye contact occurs, flush 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

• Do not rinse or wipe off the hand sanitizer before it's dry. Store in a cool dry place 1℃(34℉)~30℃(86℉)
• Avoid freezing and excessive heat above 40℃(104℉)

Inactive ingredients

Water, Aloe Barbadensis Leaf Extract, Aminomethyl Propanol, Polyacrylic Acid, Glycerin

Questions?

1-424-252-7887

Principal Display Panel – 60 mL Bottle Label

Enzysept

PREMIUM HAND SANITIZER

Kills 99.99% of germs in just 15 seconds

INSTANT KILL

Kills
99.99%
of germs

2 fl oz / 60 mL

Principal Display Panel – 500 mL Bottle Label

Enzysept

PREMIUM HAND SANITIZER

Kills 99.99% of germs in just 15 seconds

INSTANT KILL

Kills
99.99%
of germs

500 mL / 16.9 fl oz

INGREDIENTS AND APPEARANCE

ENZYSEPT 
alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 71040-101
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	86 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
Water (UNII: 059QF0KO0R)
Aloe Vera Leaf (UNII: ZY81Z83H0X)
Aminomethylpropanol (UNII: LU49E6626Q)
Polyacrylic Acid (250000 MW) (UNII: 9G2MAD7J6W)
Glycerin (UNII: PDC6A3C0OX)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 71040-101-01	60 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product	05/01/2020
2	NDC: 71040-101-02	500 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	05/01/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	05/01/2020

Labeler - HP&C, Ltd. (689847430)

Establishment
Name	Address	ID/FEI	Business Operations
HP&C, Ltd.		689847430	MANUFACTURE(71040-101)