KEKANGBEI INSTANT HAND SANITIZER- alcohol gel

kekangbei Instant hand Sanitizer by

Drug Labeling and Warnings

kekangbei Instant hand Sanitizer by is a Otc medication manufactured, distributed, or labeled by Guangdong Essence Daily Chemical Co., Ltd. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug Facts

Active ingredient

Ethyl Alcohol 75% +/-5% (V/V)

Purpose

 Antiseptic

Use

A hand sanitizer to help reduce bacteria on the skin and recomended for repeated use.

Warnings

For external use only.

Flammable,

Keep product away from fire or flame or sparks.

When using this product

do not use in or neay eyes, In case of contact, rinse eyes thoroughly with water.

Stop use and ask a doctor if

irritation or rash appears on the skin.

Keep out of reach of children.

If swallowed, get medical help or contact a Poison Control Center right away.

Directions

• Place enough to cover both hands in the palm, and rub hands together until dry
• Children under 6 years of age should be supervised bu an adult when appling this products.

Inactive ingredients

Water, Glycerin, Carbomer, Triethanolamine, Aloe Barbadensis Leaf Juice.

SPL UNCLASSIFIED SECTION

other information

• Do not store above 105 Fahrenheit.
• May discolor certain fabrics or surfaces.
• Harmful to wood finishes and plastics.

Packaging

INGREDIENTS AND APPEARANCE

KEKANGBEI INSTANT HAND SANITIZER 
alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 73931-003
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
WATER (UNII: 059QF0KO0R)
GLYCERIN (UNII: PDC6A3C0OX)
TROLAMINe (UNII: 9O3K93S3TK)
ALOE VERA LEAF (UNII: ZY81Z83H0X)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 73931-003-01	100 mL in 1 BOTTLE; Type 0: Not a Combination Product	03/31/2020
2	NDC: 73931-003-02	300 mL in 1 BOTTLE; Type 0: Not a Combination Product	03/31/2020
3	NDC: 73931-003-03	500 mL in 1 BOTTLE; Type 0: Not a Combination Product	03/31/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333E	03/31/2020

Labeler - Guangdong Essence Daily Chemical Co., Ltd (529796211)

Registrant - Guangdong Essence Daily Chemical Co., Ltd (529796211)

Establishment
Name	Address	ID/FEI	Business Operations
Guangdong Essence Daily Chemical Co., Ltd		529796211	manufacture(73931-003)