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Toasted Vanilla Sugar Hand Sanitizer Bodycology

Dosage form: liquid
Ingredients: ALCOHOL 22.5mL in 30mL
Labeler: Advanced Beauty Systems, Inc.
NDC Code: 51345-105

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.

Toasted Vanilla Sugar Hand Sanitizer

Active Ingredient purpose

Ethyl Alcohol 75% Antiseptic

Uses: to decrease bacteria on the skin.

Keep out of reach of children.

Stop use and consult a 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.
In case of accidental ingestion, seek professional assistance or contact a Poison Control Center immediately.

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 (CI77007)
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)






Bodycology

Moisturizing

Hand Sanitizer

with Aloe Vera

kills 99% of germs without water

Toasted Vanilla Sugar


30 mL 1 Fl Oz




TOASTED VANILLA SUGAR HAND SANITIZER   BODYCOLOGY
ethyl alcohol liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:51345-105
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ALCOHOL (ALCOHOL) ALCOHOL22.5 mL  in 30 mL
Inactive Ingredients
Ingredient NameStrength
PROPYLENE GLYCOL 
TROLAMINE 
GELATIN 
ALOE VERA LEAF 
FD&C RED NO. 4 
FD&C YELLOW NO. 5 
FD&C BLUE NO. 1 
D&C RED NO. 33 
Packaging
#Item CodePackage Description
1NDC:51345-105-011 BOTTLE (BOTTLE) in 1 BLISTER PACK
130 mL in 1 BOTTLE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart333E04/07/2011
Labeler - Advanced Beauty Systems, Inc. (129986613)
Registrant - Advanced Beauty Systems, Inc. (129986613)
Establishment
NameAddressID/FEIOperations
Landy International545291775manufacture(51345-105)

Revised: 06/2012
 
Advanced Beauty Systems, Inc.

Disclaimer: Every effort has been made to ensure that the information provided here is accurate, up-to-date and complete, but no guarantee is made to that effect. Drug information contained herein may be time sensitive. This information has been compiled for use by healthcare practitioners and consumers in the United States. The absence of a warning for a given drug or combination thereof in no way should be construed to indicate that the drug or combination is safe, effective or appropriate for any given patient. If you have questions about the substances you are taking, check with your doctor, nurse or pharmacist.

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