Label: AC OUT SPOT STOP SERUM- salicylic acid liquid
-
Contains inactivated NDC Code(s)
NDC Code(s): 43948-1201-1 - Packager: The Doctors Cosmetics Co., Ltd
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: unapproved drug other
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 Label Information
Updated September 25, 2012
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- ACTIVE INGREDIENT
-
INACTIVE INGREDIENT
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
- PURPOSE
- KEEP OUT OF REACH OF CHILDREN
- INDICATIONS & USAGE
- WARNINGS
- DOSAGE & ADMINISTRATION
- PRINCIPAL DISPLAY PANEL
-
INGREDIENTS AND APPEARANCE
AC OUT SPOT STOP SERUM
salicylic acid liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:43948-1201 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ) SALICYLIC ACID 0.1 mg in 100 mL Inactive Ingredients Ingredient Name Strength ALCOHOL (UNII: 3K9958V90M) BUTYLENE GLYCOL (UNII: 3XUS85K0RA) CHRYSANTHEMUM X MORIFOLIUM FLOWER (UNII: 2GR3C1A0WV) MAGNOLIA KOBUS BARK (UNII: 54LVP49595) THUJOPSIS DOLABRATA LEAFY TWIG (UNII: P24JH909CP) PUMMELO (UNII: ET1TN5W71X) CNIDIUM OFFICINALE ROOT (UNII: 8S3OZD358J) ACORUS CALAMUS ROOT (UNII: XY1K7KIQ0F) ARTEMISIA PRINCEPS LEAF (UNII: SY077EW02G) SOPHORA FLAVESCENS ROOT (UNII: IYR6K8KQ5K) PRUNUS MUME FRUIT (UNII: 639190I8CU) GLYCYRRHIZA GLABRA (UNII: 2788Z9758H) CHAMAECYPARIS OBTUSA WOOD OIL (UNII: P2OMP71Y62) CARBOMER COPOLYMER TYPE A (ALLYL PENTAERYTHRITOL CROSSLINKED) (UNII: 71DD5V995L) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:43948-1201-1 15 mL in 1 TUBE Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 09/27/2012 Labeler - The Doctors Cosmetics Co., Ltd (687479378) Registrant - The Doctors Cosmetics Co., Ltd (687479378) Establishment Name Address ID/FEI Business Operations The Doctors Cosmetics Co., Ltd 687479378 manufacture(43948-1201)