AC Out Spot stOp Serum

Dosage form: liquid
Ingredients: SALICYLIC ACID 0.1mg in 100mL
Labeler: The Doctors Cosmetics Co., Ltd
NDC Code: 43948-1201

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

salicylic acid

water, alcohol, butylene glycol, chrysanthemum morifolium flower extract, magnolia kobus bark extract, camella sinensis leaf extract, ghujopsis dolabrata branch extract, citrus grandis fruit extract, cnidium officinale root extract, acorus calamus root extract, artemisia princeps leaf extract, sophora angustifolia root extract, prunus mume fruit extract, licorice root extract, chamaecyparis obtusa water, acrylates/c10-30 alkyl acrylate crosspolymer, disodium edta, fragrance

skin proctectant

keep out of reach of the children

1.  On clean face, only apply on troubled areas. Do not rub.

 2.  When applying on top of a make up, use tip of the tube

      to apply and soothe troubled areas quickly

When using this product
- keep out of eyes, ears, and mouth.  If contact occurs, rinse with plenty of cold water right away and contact a physician.  If swallowing, drink plenty of water and contact a physician

for external use only

AC OUT SPOT STOP SERUM 
salicylic acid liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:43948-1201
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
SALICYLIC ACID (SALICYLIC ACID) SALICYLIC ACID0.1 mg  in 100 mL
Inactive Ingredients
Ingredient NameStrength
ALCOHOL 
BUTYLENE GLYCOL 
CHRYSANTHEMUM X MORIFOLIUM FLOWER 
MAGNOLIA KOBUS BARK 
THUJOPSIS DOLABRATA LEAFY TWIG 
PUMMELO 
CNIDIUM OFFICINALE ROOT 
ACORUS CALAMUS ROOT 
ARTEMISIA PRINCEPS LEAF 
SOPHORA FLAVESCENS ROOT 
PRUNUS MUME FRUIT 
GLYCYRRHIZA GLABRA 
CHAMAECYPARIS OBTUSA WOOD OIL 
CARBOMER COPOLYMER TYPE A (ALLYL PENTAERYTHRITOL CROSSLINKED) 
Packaging
#Item CodePackage Description
1NDC:43948-1201-115 mL in 1 TUBE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
unapproved drug other09/27/2012
Labeler - The Doctors Cosmetics Co., Ltd (687479378)
Registrant - The Doctors Cosmetics Co., Ltd (687479378)
Establishment
NameAddressID/FEIOperations
The Doctors Cosmetics Co., Ltd687479378manufacture(43948-1201)

Revised: 09/2012
 
The Doctors Cosmetics Co., Ltd

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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