BODYCOLOGY SWEET PETALS- ethyl alcohol gel 
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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Sweet Petals Hand Sanitizer

Active Ingredient                             purpose

Ethyl Alcohol 70%                           Antiseptic

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)
image of bottle

bodycology

moisturizing

hand sanitizer  with aloe vera

sweet petals


30 mL e 1 FL OZ





image of blister

BODYCOLOGY  SWEET PETALS
ethyl alcohol gel
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:49035-985
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL70 mL  in 100 mL
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
CARBOMER INTERPOLYMER TYPE A (55000 MPA.S)) (UNII: 59TL3WG5CO)  
TROLAMINE (UNII: 9O3K93S3TK)  
GELATIN (UNII: 2G86QN327L)  
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 CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:49035-985-021 in 1 BOTTLE
1NDC:49035-985-0130 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: 4/2011
Document Id: f0ecca61-e1cf-4b2e-bf72-9d91ae2a4652
Set id: b7f08073-f054-4c96-b6c7-f3bb857cb91c
Version: 1
Effective Time: 20110411
 
Wal-Mart Stores, Inc.