HAND SANITIZER- ethyl alcohol lotion

Hand Sanitizer by

Drug Labeling and Warnings

Hand Sanitizer by is a Otc medication manufactured, distributed, or labeled by E.CIS COSMETIC.Co.,Ltd. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient(s)

Ethyl Alcohol 62% v/v. Purpose: Antiseptic

Purpose

Antiseptic, Hand Sanitizer

Use

Health care personnel hand rub to help reduce bacteria that potentially can cause disease.

Warnings

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

Do not use

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

WHEN USING

When using this product keep out of eyes, ears, and mouth. In case of contact with eyes, rinse eyes thoroughly with water.

STOP USE

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

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 15-30C (59-86F)
• Avoid freezing and excessive heat above 40C (104F)

Inactive ingredients

Water, Cetyl Alcohol, Glycerin, Caprylic/Capric Triglyceride, Acrylates Copolymer, Olea Europaea (Olive) Fruit Oil, Carbomer, Aminomethyl Propanol, Fragrance, Styrene/Acrylates Copolymer, Sodium Hyaluronate, Propolis Extract, Panthenol, 1,2-Hexanediol, Butylene Glycol, Honey Extract, Macadamia Ternifolia Seed Oil, Butyrospermum Parkii (Shea) Butter, Ascorbic Acid, Tocopheryl Acetate, Royal Jelly Extract, Aloe Barbadensis Leaf Extract

Package Label - Principal Display Panel

HanBee
Just Bee Sure
Hand Sanitizer Moisturizing Serum
Ethyl Alcohol 62%
Contains Royal Jelly
Deep Moisturizing Natural Nourishing
Gentle for the Whole Family
500 mL (16.9 fl. oz.)

INGREDIENTS AND APPEARANCE

HAND SANITIZER 
ethyl alcohol lotion

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 73862-224
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	62 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
GLYCERIN (UNII: PDC6A3C0OX)
WATER (UNII: 059QF0KO0R)
OLIVE OIL (UNII: 6UYK2W1W1E)
CARBOMER 940 (UNII: 4Q93RCW27E)
BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
ROYAL JELLY (UNII: L497I37F0C)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
AMINOMETHYLPROPANOL (UNII: LU49E6626Q)
STYRENE/ACRYLAMIDE COPOLYMER (MW 500000) (UNII: 5Z4DPO246A)
HYALURONATE SODIUM (UNII: YSE9PPT4TH)
1,2-HEXANEDIOL (UNII: TR046Y3K1G)
HONEY (UNII: Y9H1V576FH)
MACADAMIA OIL (UNII: 515610SU8C)
ALPHA-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
BUTYL ACRYLATE/METHYL METHACRYLATE/METHACRYLIC ACID COPOLYMER (18000 MW) (UNII: JZ1374NL9E)
ASCORBIC ACID (UNII: PQ6CK8PD0R)
SHEA BUTTER (UNII: K49155WL9Y)
PROPOLIS WAX (UNII: 6Y8XYV2NOF)
PANTHENOL (UNII: WV9CM0O67Z)
MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 73862-224-02	24 in 1 CARTON	03/03/2020
1	NDC: 73862-224-01	500 mL in 1 BOTTLE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	03/03/2020

Labeler - E.CIS COSMETIC.Co.,Ltd (689846270)

Establishment
Name	Address	ID/FEI	Business Operations
E.CIS COSMETIC.Co.,Ltd		689846270	manufacture(73862-224)