Label: SCAR DIMINISHING CREAM cream

  • NDC Code(s): 83675-018-01
  • Packager: Guangzhou Hanhai Trading 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 October 7, 2023

If you are a consumer or patient please visit this version.

  • Active Ingredient

    Camphor 13.0%

  • Purpose

  • Purpose

    Scar Diminishing

  • Use

    scar removat aram mihimie soar
    and mhomce the shin's clasticity

  • Warnings

    For external use only. Do not take it internally.

    Keep Out Of Reach Of Children
    Sensitive Skin

  • Do not use

    Product shall not be eat

  • When Using

    After cleaning the abdomen .take appropriate gel evenlyon the abdomen

  • Stop Use

    In case of adverse reactions, please stop using this product.If the symptoms.

  • Ask Doctor

    ask doctor in case of Sensitive Skin

  • Keep Oot Of Reach Of Children

    Keep Out Of Reach Of Children

  • Directions

    After cleaning the abdomen .take appropriate gel evenlyon the abdomen

  • Other information

    Store the product in a cool, dry and well-ventilated place

    Avoid direct sunlight

  • Inactive ingredients

    Silicone

    Mint

  • PRINCIPAL DISPLAY PANEL

    01

  • INGREDIENTS AND APPEARANCE
    SCAR DIMINISHING CREAM 
    scar diminishing cream cream
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:83675-018
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    CAMPHOR (NATURAL) (UNII: N20HL7Q941) (CAMPHOR (NATURAL) - UNII:N20HL7Q941) CAMPHOR (NATURAL)13 g  in 100 g
    Inactive Ingredients
    Ingredient NameStrength
    ARCHANGELENONE (UNII: AG84U27TWU)  
    MINT (UNII: FV98Z8GITP)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:83675-018-0120 g in 1 BOX; Type 0: Not a Combination Product10/06/2023
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved drug other10/06/2023
    Labeler - Guangzhou Hanhai Trading Co., Ltd (419707381)
    Establishment
    NameAddressID/FEIBusiness Operations
    Guangzhou Hanhai Trading Co., Ltd419707381label(83675-018) , manufacture(83675-018)