BLUE CEDAR HAND SANITIZER- hand sanitizer gel

Blue Cedar Hand Sanitizer by

Drug Labeling and Warnings

Blue Cedar Hand Sanitizer by is a Otc medication manufactured, distributed, or labeled by Anhui Kiwi Biotech Co., Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

DOSAGE & ADMINISTRATION

Store below 110°F (43° C).
May discolor certain fabrics or surfaces.

WARNINGS

Flammable. Keep away from fire or flame.

Forexternal use only.

Do not use this product in or near the eyes. In case of accidental contact, ninse eyes thoroughly with water.

Stop use and ask doctor if iritation or rash appears andlasts.

Keep away from children. If sallowed, get medicalhelp right away,

PURPOSE

Kills Harmful Bacteria or Germs

KEEP OUT OF REACH OF CHILDREN

keep out of reach of children.

INDICATIONS & USAGE

Place enough product (1.5~-2 mL, about one full pump) in your palm to thoroughly cover your hands.

Rub hands briskly until dry.

Children under 6 years old should be supervised when using this product.

ACTIVE INGREDIENT

Ethyl Alcohol 75土 59% 6(VW) or 65士5%

INACTIVE INGREDIENT

Water, Carbomer, Glycereth :26, Triethanolamine, Fragrance (Parfum).

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

BLUE CEDAR HAND SANITIZER 
hand sanitizer gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 55444-003
Route of Administration	EXTRACORPOREAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	150 mL  in 200 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
.ALPHA.-HEXYLCINNAMALDEHYDE (UNII: 7X6O37OK2I)
.ALPHA.-TERPINEOL (UNII: 21334LVV8W)
TERPINEOL (UNII: R53Q4ZWC99)
.GAMMA.-NONALACTONE (UNII: I1XGH66S8P)
LINALOOL, (+/-)- (UNII: D81QY6I88E)
METHYL DIHYDROJASMONATE (SYNTHETIC) (UNII: 3GW44CIE3Y)
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)
TROLAMINE (UNII: 9O3K93S3TK)
GLYCERETH-26 (UNII: NNE56F2N14)
PHENYLETHYL ALCOHOL (UNII: ML9LGA7468)

Product Characteristics
Color		Score
Shape		Size
Flavor	FRUIT	Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 55444-003-01	200 mL in 1 BOTTLE; Type 0: Not a Combination Product	03/21/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved drug other		03/21/2020

Labeler - Anhui Kiwi Biotech Co., Ltd. (554444636)

Establishment
Name	Address	ID/FEI	Business Operations
Anhui Kiwi Biotech Co., Ltd.		554444636	manufacture(55444-003)