MANGO MADNESS HAND SANITIZER- alcohol solution

Mango Madness Hand Sanitizer by

Drug Labeling and Warnings

Mango Madness Hand Sanitizer by is a Otc medication manufactured, distributed, or labeled by Brands International. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug Facts

Active Ingredients

Ethyl Alcohol 62%

Purpose

Antiseptic

Uses

• To decrease bacteria on the skin and clean hands.
• Recommended for repeated use.

Warnings

For external use only.

Flammable. Keep away from fire or flame.

KEEP OUT OF REACH OF CHILDREN

Keep out of reach of children. If accidentally swallowed, get medical help or contact a Poison Control Center right away.

WHEN USING

Do not get into eyes. If contact occurs, rinse thoroughly with water.

STOP USE

Discontinue use if irritation or redness develop. If irritation persists for more than 72 hours, consult a doctor.

Directions

• apply to hands until thoroughly wet
• rub vigorously until dry
• supervise children in the use of this product.

Other information

• may discolor certain fabrics or surfaces.
• do not store above 110°F (43°C)

Inactive ingredients

Water, Isopropyl Alcohol, Glycerin, Carbomer, Aminomethyl Propanol, Fragrance, Propylene Glycol, Isopropyl Myristate, Aloe Barbadensis Leaf Juice, Tocopheryl (Vitamin E) Acetate, Sunflower (Helianthus Annus) Seed Extract, Grapefruit (Citrus Grandis) Seed Extract, Yellow 5 (CI 19140), Yellow 6 (CI 15985), Red 40 (CI 16035).

SPL UNCLASSIFIED SECTION

Manufactured by:

Brands International Corp.
Markham, ON, L6G 1B9 Canada
www.brandsicorp.com

Package Label

Mango Madness

ANTIBACTERIAL

Hand Sanitizer Gel

Kills 99.99% of Germs
1 FL OZ (29 ml)

INGREDIENTS AND APPEARANCE

MANGO MADNESS HAND SANITIZER 
alcohol solution

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 50157-107
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)
ISOPROPYL ALCOHOL (UNII: ND2M416302)
GLYCERIN (UNII: PDC6A3C0OX)
CARBOMER HOMOPOLYMER TYPE C (ALLYL PENTAERYTHRITOL CROSSLINKED) (UNII: 4Q93RCW27E)
AMINOMETHYLPROPANOL (UNII: LU49E6626Q)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
SUNFLOWER SEED (UNII: R9N3379M4Z)
CITRUS PARADISI SEED (UNII: 12F08874Y7)
FD&C YELLOW NO. 5 (UNII: I753WB2F1M)
FD&C YELLOW NO. 6 (UNII: H77VEI93A8)
FD&C RED NO. 40 (UNII: WZB9127XOA)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 50157-107-01	29 mL in 1 BOTTLE; Type 0: Not a Combination Product	04/20/2015

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333E	04/20/2015

Labeler - Brands International (243748238)