ENCHANTED FOREST HAND SANITIZER BODYCOLOGY- ethyl alcohol liquid

Enchanted Forest Hand Sanitizer by

Drug Labeling and Warnings

Enchanted Forest Hand Sanitizer by is a Otc medication manufactured, distributed, or labeled by Advanced Beauty Systems, Inc., Landy International. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Active Ingredient    Purpose
Ethyl Alcohol 75%    Antiseptic

Uses: To decrease bacteria on the skin.

Keep out of reach of children. In case of accidental ingestion, seek professional assistance or contact a Poison Control Center immediately.

Stop use and consult doctor if irritation and redness develop and persist for more than 72 hours.

Warnings
For external use only.

FLAMMABLE. Keep away from heat and flame.

When using this product
-Avoid contact with eyes. If contact occurs, flush eyes with water.
-Avoid contact with broken skin.

Directions
-Wet hands with product.
-Briskly rub hands together until dry.
-For children under 6, use only under adult supervision.
-Not recommended for infants.

Inactive ingredients Water (Aqua, Eau), Fragrance (parfum), propylene glycol, Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Triethanolamine, Gelatin, Tocopheryl Acetate, Aloe Barbadensis Leaf Juice, Ultramarines (CI 77007)
May Contain: FD and C No.4 (CI 14700), FD and C Yellow No. 5 (CI 19140) FD and C Blue No. 1 (CI 42090), D and C Red No. 33 (CI 17200)

PRINCIPAL DISPLAY PANEL

Bodycology
MOISTURIZING HAND SANITIZER
with Aloe Vera
kills 99% of germs without water
Enchanted Forest

30mL    1 FL OZ

INGREDIENTS AND APPEARANCE

ENCHANTED FOREST HAND SANITIZER  BODYCOLOGY
ethyl alcohol liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 51345-051
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	22.5 mL  in 30 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
TROLAMINE (UNII: 9O3K93S3TK)
GELATIN (UNII: 2G86QN327L)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
FD&C RED NO. 4 (UNII: X3W0AM1JLX)
FD&C YELLOW NO. 5 (UNII: I753WB2F1M)
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
D&C RED NO. 33 (UNII: 9DBA0SBB0L)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 51345-051-01	1 in 1 BLISTER PACK
1		30 mL in 1 BOTTLE

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part333E	04/07/2011

Labeler - Advanced Beauty Systems, Inc. (129986613)

Registrant - Advanced Beauty Systems, Inc. (129986613)

Establishment
Name	Address	ID/FEI	Business Operations
Landy International		545291775	manufacture(51345-051)