Bodycology Vanilla Cupcake

Dosage form: gel
Ingredients: ALCOHOL 70mL in 100mL
Labeler: Wal-Mart Stores, Inc.
NDC Code: 49035-992

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.

Vanilla Cupcake Hand Sanitizer

Active Ingredient                             purpose

Ethyl Alcohol 70%                          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 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 (Aloe Vera leaf juice), Ultramarines (CI77007)
May contain: FD C Red No.4(CI 14700, Aka504), FD C Yellow No. 5 (CI 19140,Ki4), FD C Blue No.1 (CI 42090, Ao1), D C Red No 33(CI 17200,Aka227)



Bodycology

Moisturizing Hand Sanitizer

30 mL 1 Fl Oz



BODYCOLOGY  VANILLA CUPCAKE
ethyl alcohol gel
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:49035-992
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ALCOHOL (ALCOHOL) ALCOHOL70 mL  in 100 mL
Inactive Ingredients
Ingredient NameStrength
WATER 
PROPYLENE GLYCOL 
CARBOMER INTERPOLYMER TYPE A (55000 MPA.S)) 
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:49035-992-021 BOTTLE (BLISTER PACK) in 1 BOTTLE
1NDC:49035-992-0130 mL in 1 BOTTLE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333E04/09/2011
Labeler - Wal-Mart Stores, Inc. (051957769)

Revised: 04/2011
 
Wal-Mart Stores, 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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