Label: HOSPICARE 40R ADULT BODY WIPES- wet wipes cloth

  • NDC Code(s): 84215-004-01
  • Packager: Freshening Paper Products(Hui Zhou)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 April 8, 2024

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

  • Active Ingredient(s)

    Chlorhexidine digluconate:0.10%

  • Purpose

    FOR DRY BATH, BODY MASSAGE, LARGE BODY SURFACE & HEAVY-DUTY CL EANING

  • Use

    ●Extra-large towel size for ease of cleaning
    ●Strong and tear resistant for surface cleaning yet gentle on skin
    ●Improves patient care and satisfaction
    ●Eliminates odour associated with incontinence changes
    ●Eliminates use of harsh soaps, rough washcloths and towel drying
    ●Helps you stay cool, clean, comfortable and refreshed
    anytime, anywhere

  • Warnings

    Discard used wipe in trash. Do not fush in tilt

  • Do not use

    ●For extemal use only.

    ●For adults and childen 2 years and older.

  • WHEN USING

    Avoid contact with eyes

  • STOP USE

    ●Skin imitation is uncommon but should a reaction occur, discontinue use immediately.

  • KEEP OUT OF REACH OF CHILDREN

    Keep out of reach of children.

  • Directions

    使用本产品时,请监督 6 岁以下儿童,避免吞咽。

  • Other information

    Expiny date is 36 months from MFG dato MFG (DDMMMYY)

  • Inactive ingredients

    Purified Water, Phenoxyethanol, Aloe barbadensis leaf juice, Sodium gluconate, Chlorphenesin, Polysorbate 20, Chlorhexidine digluconate, Fragrance, Glycerin

  • Package Label - Principal Display Panel

    label

  • INGREDIENTS AND APPEARANCE
    HOSPICARE 40R ADULT BODY WIPES 
    wet wipes cloth
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:84215-004
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    CHLORHEXIDINE GLUCONATE (UNII: MOR84MUD8E) (CHLORHEXIDINE - UNII:R4KO0DY52L) CHLORHEXIDINE GLUCONATE0.1 g  in 100 
    Inactive Ingredients
    Ingredient NameStrength
    POLYSORBATE 20 (UNII: 7T1F30V5YH)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    PHENOXYETHANOL (UNII: HIE492ZZ3T)  
    SODIUM GLUCONATE (UNII: R6Q3791S76)  
    WATER (UNII: 059QF0KO0R)  
    CHLORPHENESIN (UNII: I670DAL4SZ)  
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:84215-004-0140 in 1 BAG; Type 0: Not a Combination Product04/11/2024
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved drug other04/09/2024
    Labeler - Freshening Paper Products(Hui Zhou)Co.Ltd (723246894)
    Establishment
    NameAddressID/FEIBusiness Operations
    Freshening Paper Products(Hui Zhou)Co.Ltd723246894manufacture(84215-004)