AWAKEN BY QUALITY CHOICE HAND SANITIZER CITRUS COCONUT- ethyl alcohol liquid

Awaken by Quality Choice Hand Sanitizer by

Drug Labeling and Warnings

Awaken by Quality Choice Hand Sanitizer by is a Otc medication manufactured, distributed, or labeled by Chain Drug Marketing Association Inc, Apollo Health and Beauty Care. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active ingredient

Ethyl Alcohol 65%

Purpose

Antiseptic

Uses

helps eliminate bacteria on hands.

Warnings

For external use only.

• Flammable.
• Keep away from source of heat or fire.

When using this product

avoid contact with eyes. If contact occurs, rinse thoroughly with water.

Stop use and ask a doctor if

irritation or redness develops and lasts.

Keep out of reach of children.

In case of accidental ingestion, get medical help or contact a Poison Control Center immediately.

Directions

Put enough product in your palm to cover hands and rub hands together until dry. Children under 6 years should be supervised when using this product.

Other information

• store at a temperature below 110°F (43°C).
• may discolor certain fabrics or surfaces.

Inactive ingredients

Water (Aqua), Fragrance (Parfum), Carbomer, Glycerin, Isopropyl Myristate, Isopropyl Alcohol, Aminomethyl Propanol, Aloe Barbadensis Leaf Juice, Mannitol, Cellulose, Tocopheryl Acetate, Hydroxypropyl Methylcellulose, PEG-60 Almond Glycerides, Chromium Hydroxide Green (CI 77289), Yellow 5 (CI 19140).

Questions or comments?

1-284-449-9300

Label Copy

INGREDIENTS AND APPEARANCE

AWAKEN BY QUALITY CHOICE HAND SANITIZER  CITRUS COCONUT
ethyl alcohol liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 63868-481
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	650 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
CARBOMER 934 (UNII: Z135WT9208)
GLYCERIN (UNII: PDC6A3C0OX)
ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)
ISOPROPYL ALCOHOL (UNII: ND2M416302)
AMINOMETHYLPROPANOL (UNII: LU49E6626Q)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
MANNITOL (UNII: 3OWL53L36A)
POWDERED CELLULOSE (UNII: SMD1X3XO9M)
.ALPHA.-TOCOPHEROL ACETATE, DL- (UNII: WR1WPI7EW8)
HYPROMELLOSES (UNII: 3NXW29V3WO)
PEG-60 ALMOND GLYCERIDES (UNII: 4Y0E651N0F)
CHROMIUM HYDROXIDE GREEN (UNII: RV8FT8XF5R)
FD&C YELLOW NO. 5 (UNII: I753WB2F1M)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 63868-481-08	259 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	08/18/2016

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333E	08/18/2016

Labeler - Chain Drug Marketing Association Inc (011920774)

Registrant - Apollo Health and Beauty Care (201901209)

Establishment
Name	Address	ID/FEI	Business Operations
Apollo Health and Beauty Care		201901209	manufacture(63868-481)