WINTER VANILLA HAND SANITIZER BODYCOLOGY (ALCOHOL) LIQUID [WAL-MART STORES INC]

WINTER VANILLA HAND SANITIZER BODYCOLOGY (ALCOHOL) LIQUID [WAL-MART STORES INC]
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NDC	49035-109-01, 49035-109-02
Set ID	fcbd0464-9d53-40a8-922b-8dc473790642
Category	HUMAN OTC DRUG LABEL
Packager	Wal-Mart Stores Inc
Generic Name
Product Class
Product Number
Application Number	PART333E

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ACTIVE INGREDIENT

Active ingredient purpose

Alcohol 75% Antiseptic

Uses For hand washing 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.

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

Warnings

For external use only.

FLAMMABLE. Keep away from flame or high heat.

When using this product

Avoid contact with eyes. If contact occurs, flush eyes with water.

Avoid contact with broken skin

Directions

Wet hands thoroughly with product and allow to dry without wiping.

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&C Red No. 4 (CI 14700), FD&C Yellow No. 5 (CI 19140), FD&C Blue No. 1 (CI 42090), D&C Red No. 33 (CI 17200).
PRINCIPAL DISPLAY PANEL

limited time only

bodycology hand sanitizer

1 Fl Oz. 30 mL

INGREDIENTS AND APPEARANCE

WINTER VANILLA HAND SANITIZER BODYCOLOGY
alcohol liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:49035-109
Route of Administration	TOPICAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	75 in 100 mL

Ingredient Name	Strength
Inactive Ingredients
WATER (UNII: 059QF0KO0R)
CARBOMER COPOLYMER TYPE A (ALLYL PENTAERYTHRITOL CROSSLINKED) (UNII: 71DD5V995L)
TROLAMINE (UNII: 9O3K93S3TK)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
GELATIN (UNII: 2G86QN327L)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
ULTRAMARINE BLUE (UNII: I39WR998BI)
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)

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:49035-109-02	1 in 1 PACKAGE
1	NDC:49035-109-01	30 mL in 1 BOTTLE, PLASTIC

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC monograph not final	part333E	05/22/2013

Labeler - Wal-Mart Stores Inc (051957769)

Registrant - Wal-Mart Stores Inc (051957769)

Name	Address	ID/FEI	Business Operations
Establishment
Landy International		545291775	manufacture(49035-109)

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