AURAFRESH INSTANT HAND SANITIZER WITH ALOE AND VITAMIN E LAVENDER- alcohol gel

aurafresh instant hand sanitizer with aloe and vitamin e by

Drug Labeling and Warnings

aurafresh instant hand sanitizer with aloe and vitamin e by is a Otc medication manufactured, distributed, or labeled by Ningbo Pulisi Daily Chemical Products Co., Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Active ingredient                                  Purpose

Ethyl Alcohol                62%      ...        Antiseptic

PURPOSE

Hand sanitizer to help decrease bacteria on the skin.

KEEP OUT OF REACH OF CHILDREN

If swallowed, get medical help or contact local poison control center right away.

Children under 6 years of age should be supervised by an adult when using.

INDICATIONS & USAGE

when using this product, avoid contact with face, eyes and broken skin. In case of eye contact, flush with plenty of water and seek medical advice.

WARNINGS

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

Stop using and ask a doctor, if irritation and redness develops.

DOSAGE & ADMINISTRATION

wet hands thoroughly with product and rub into skin until dry.

INACTIVE INGREDIENT

Water, Carbomer, Glycerin, Propylene Glycol, Triethanolamine, Aloe Barbadensis Leaf Juice, Tocopheryl Acetate, Fragrance, red 33, blue 1

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

AURAFRESH INSTANT HAND SANITIZER WITH ALOE AND VITAMIN E  LAVENDER
alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 40104-286
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
WATER (UNII: 059QF0KO0R)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
GLYCERIN (UNII: PDC6A3C0OX)
.ALPHA.-TOCOPHEROL ACETATE, D- (UNII: A7E6112E4N)
TROLAMINE (UNII: 9O3K93S3TK)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 40104-286-01	53 mL in 1 BOTTLE; Type 0: Not a Combination Product	08/10/2017

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	08/10/2017

Labeler - Ningbo Pulisi Daily Chemical Products Co., Ltd. (529047265)

Registrant - Ningbo Pulisi Daily Chemical Products Co., Ltd. (529047265)

Establishment
Name	Address	ID/FEI	Business Operations
Ningbo Pulisi Daily Chemical Products Co., Ltd.		529047265	manufacture(40104-286)