You are here: Home > Over-the-counter (OTC) Drugs > B > Bodycologyvanilla Cupcake (Wal-mart Stores, Inc.)

Name:Bodycologyvanilla Cupcake
Manufacturer:Wal-mart Stores, Inc.
Category:Over-the-counter (OTC) Marketed Drugs


Vanilla Cupcake Hand Sanitizer

BODYCOLOGY VANILLA CUPCAKE - 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.

----------

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)


Image of bottle label

Bodycology

Moisturizing Hand Sanitizer

30 mL 1 Fl Oz



Image of blister label


BODYCOLOGY  VANILLA CUPCAKE
ethyl alcohol gel
Product Information
Product Type HUMAN OTC DRUG Item Code (Source) NDC:49035-992
Route of Administration TOPICAL DEA Schedule     
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
ALCOHOL (ALCOHOL) ALCOHOL 70 mL  in 100 mL
Inactive Ingredients
Ingredient Name Strength
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  
Product Characteristics
Color      Score     
Shape Size
Flavor Imprint Code
Contains     
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:49035-992-02 1 BOTTLE ( BLISTER PACK) in 1 BOTTLE contains a BOTTLE (49035-992-01)
1 NDC:49035-992-01 30 mL in 1 BOTTLE This package is contained within the BOTTLE (49035-992-02)

Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
OTC monograph not final part333E 04/09/2011

Labeler - Wal-Mart Stores, Inc. (051957769)

Revised: 04/2011 Wal-Mart Stores, Inc.



Source: http://dailymed.nlm.nih.gov
Reproduced with permission of U.S. National Library of Medicine


Copyright © 2019 Drugsdb.eu by Dionisios Fentas || Terms of Use

Loading

OTC Marketed Drugs Alphabetically
A| B| C| D| E| F| G| H| I| J| K| L| M| N| O| P| Q| R| S| T| U| V| W| X| Y| Z| 0-9

Categories:
Prescription(RX) Drugs
Over-the-counter (OTC) Drugs
Homeopathic Drugs
Animal Drugs
Feedback