HAND SANITIZER PREVAIL- alcohol spray

Hand Sanitizer by

Drug Labeling and Warnings

Hand Sanitizer by is a Otc medication manufactured, distributed, or labeled by Creation's Garden Natural Products, Inc. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Ethyl Alcohol 62%.................................Antiseptic

Uses

• To decrease bacteria on the skin that could cause disease.

• Recommended for repeated use.
  

Warnings

When using this product:

• Keep out of eyes. In case of contact with eyes, flush thoroughly with water
• Avoid contact with broken skin
• For external use only-skin
• Flammable. Keep away from heat and flame.
• Stop use and ask doctor if skin irritation develops
  

Keep out of reach of children

In case of accidental ingestion, seek professional assistance or contact a Poison Control Center immediately

Directions

• Wet skin area with product
• Rub hands together until dry
• supervise children with the use of this product
  

Other information

Do not store above 105°F. May discolor some fabrics. Harmful to wood finishes and plastics.

Inactive ingredients

Water, Propylene Glycol, Glycerin, Carbomer, Isopropyl Myristate, Tocopheryl (Vitamin E) Acetate, Aloe Barbadensis Leaf Juice, Aminomethyl Propanol, Yellow 5, Fragrance

Questions

(866) 375-6925

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

HAND SANITIZER  PREVAIL
alcohol spray

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 24488-005
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	4.58 mL  in 7.39 mL

Inactive Ingredients
Ingredient Name	Strength
Water (UNII: 059QF0KO0R)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
GLYCERIN (UNII: PDC6A3C0OX)
ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)
ALPHA-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
AMINOMETHYLPROPANOL (UNII: LU49E6626Q)
FD&C YELLOW NO. 5 (UNII: I753WB2F1M)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 24488-005-52	7.39 mL in 1 BOTTLE, SPRAY

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved drug other		04/12/2010

Labeler - Creation's Garden Natural Products, Inc (839471216)

Registrant - Creation's Garden Natural Products, Inc (839471216)

Establishment
Name	Address	ID/FEI	Business Operations
Creation's Garden Natural Products, Inc		839471216	manufacture