WINTER VANILLA HAND SANITIZER BODYCOLOGY- alcohol liquid 
Wal-Mart Stores Inc

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

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winter vanilla hand sanitizer

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).

carton

bottle

limited time only

bodycology hand sanitizer

1 Fl Oz. 30 mL

WINTER VANILLA HAND SANITIZER  BODYCOLOGY
alcohol liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:49035-109
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL75   in 100 mL
Inactive Ingredients
Ingredient NameStrength
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)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:49035-109-021 in 1 PACKAGE
1NDC:49035-109-0130 mL in 1 BOTTLE, PLASTIC
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333E05/22/2013
Labeler - Wal-Mart Stores Inc (051957769)
Registrant - Wal-Mart Stores Inc (051957769)
Establishment
NameAddressID/FEIBusiness Operations
Landy International545291775manufacture(49035-109)

Revised: 5/2013
Document Id: c4bee47e-a5be-4159-b419-fe5725843021
Set id: fcbd0464-9d53-40a8-922b-8dc473790642
Version: 1
Effective Time: 20130522
 
Wal-Mart Stores Inc