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VFB BIO PEEL

Dosage form: powder
Ingredients: ALUMINUM OXIDE 6.5mg in 1g
Labeler: General Bio Co., Ltd.
NDC Code: 69422-2001

Disclaimer: This drug has not been found by FDA to be safe and effective, and this labeling has not been approved by FDA. For further information about unapproved drugs, click here.

Drug Facts

ALUMINA

LAVENDER FLOWER EXT, MATRICARIA LEAF EXT, PEPPERMINT EXT, SPEARMINT EXT, ETC.


skin protectant



keep out of reach of the children

USE WITH BIO PEEL SOLUTION


・Stop using the product when you have skin problems or the product disagrees with your skin
・Stop using the product immediately and consult a dermatologist if you have redness, swelling, itching or irritation on the skin while or after using the product.
・If the product gets into the eyes, don't rub but rinse with water.
・Don't place the product in any place where it will be subjected to extremely high or low temperatures or direct sunlight.


for external use only

VFB BIO PEEL 
aluminum oxide powder
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:69422-2001
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ALUMINUM OXIDE (ALUMINUM OXIDE) ALUMINUM OXIDE6.5 mg  in 1 g
Inactive Ingredients
Ingredient NameStrength
LAVANDIN OIL 
MENTHA PIPERITA 
MENTHA SPICATA 
Packaging
#Item CodePackage Description
1NDC:69422-2001-10.4 g in 1 BOTTLE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
unapproved drug other12/09/2014
Labeler - General Bio Co., Ltd. (688299527)
Registrant - General Bio Co., Ltd. (688299527)
Establishment
NameAddressID/FEIOperations
General Bio Co., Ltd.688299527manufacture(69422-2001)

 
General Bio Co., Ltd.

Medically reviewed on Dec 11, 2017

Further information

Always consult your healthcare provider to ensure the information displayed on this page applies to your personal circumstances.

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