Label: ECHO PEARL ANTISEPTIC HAND WASH- benzalkonium chloride liquid

  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: OTC monograph not final

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.

Drug Label Information

Updated May 21, 2020

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

  • Drug Facts

  • PURPOSE

    Purpose: Antiseptic

  • ACTIVE INGREDIENTS

    Component

    Benzalkonium chloride - 0.2 %

  • INACTIVE INGREDIENTS

    Lauryl alcohol ethoxylate, Methyl ester sulfonate, Sodium chloride, Vitamin E, Citric acid, Water, Boro glycerine, Clove oil.

  • Use: This product is a specially formulated hand wash soap for hygiene hand washing which leaves the skin soft and smooth, and decrease microbes on the skin.

  • Directions: Wet hand with fresh water and apply soap. Rub hands together for 20 sec. Rinse hands thoroughly with fresh water.

  • When using this product: keep out of eyes, ears, and mouth. In case of contact with eyes, rinse eyes thoroughly with water.

    Stop use and ask a doctor: if irritation occurs, please consult a doctor.

    Do not use

    • In children less than 2 months of age

    • On open skin wounds.

    Warning

    • For external use only

    • Keep out of Reach of Children

  • Other information

    • Store between 15-30°C (59-86°F)

    • Avoid freezing and excessive heat above 40°C (104°F)

  • SPL UNCLASSIFIED SECTION

    9001: 2015

    ISO CERTIFIED COMPANY

    Manufactured by:
    Atlantic Care Chemicals. Pvt. Ltd
    Industrial Development Plot,
    Alappuzha, Kerala, India.

    PASSION FOR INNOVATION

    care@atlanticchemicals.com
    www.atlanticchemicals.com

    MADE IN INDIA

  • Packaging

    Epearl1

  • INGREDIENTS AND APPEARANCE
    ECHO PEARL ANTISEPTIC HAND WASH 
    benzalkonium chloride liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:77249-105
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE2 g  in 1 L
    Inactive Ingredients
    Ingredient NameStrength
    LAURYL ALCOHOL (UNII: 178A96NLP2)  
    S-METHYL METHANETHIOSULFONATE (UNII: 0906Z2356U)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    .ALPHA.-TOCOPHEROL (UNII: H4N855PNZ1)  
    CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
    WATER (UNII: 059QF0KO0R)  
    BOROGLYCERIN (UNII: U3LMU4AN21)  
    CLOVE OIL (UNII: 578389D6D0)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:77249-105-455 L in 1 CAN; Type 0: Not a Combination Product05/15/2020
    2NDC:77249-105-010.1 L in 1 BOTTLE; Type 0: Not a Combination Product05/15/2020
    3NDC:77249-105-020.2 L in 1 BOTTLE; Type 0: Not a Combination Product05/15/2020
    4NDC:77249-105-050.5 L in 1 BOTTLE; Type 0: Not a Combination Product05/15/2020
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333A05/15/2020
    Labeler - ATLANTIC CARE CHEMICALS PRIVATE LIMITED (861499902)
    Establishment
    NameAddressID/FEIBusiness Operations
    ATLANTIC CARE CHEMICALS PRIVATE LIMITED861499902manufacture(77249-105)