Label: SWEET CAREFOR ALCOHOL WIPES- alcohol cloth

  • NDC Code(s): 52489-001-01, 52489-001-02, 52489-001-03, 52489-001-04, view more
    52489-001-05, 52489-001-06, 52489-001-07, 52489-001-08, 52489-001-09, 52489-001-10, 52489-001-11, 52489-001-12, 52489-001-13, 52489-001-14, 52489-001-15, 52489-001-16, 52489-001-17, 52489-001-18, 52489-001-19
  • Packager: Imperial Palace Commodity(shenzhen)CO.,LTD
  • Category: HUMAN OTC DRUG LABEL

Drug Label Information

Updated November 20, 2023

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  • SPL UNCLASSIFIED SECTION

    DRUG FACTS

  • Active Ingredient(s)

    • Alcohol 75% v/v.
  • Purpose

    • Cleaning and disinfection
  • Uses

    Packs

    • Peel back lid and then label.
    • Remove wipes as required.
    • Replace lid and label to keep wipes moist.

    Buckets

    • Open the bucket lid from the top.
    • Locate tear cut in the inner pouch, tear straight to open. Do not remove wipesroll from pouch.
    • Pull first wipes from center of roll up through opening.
    • Thread first wipe through dispensing nozzle in top of roll.
    • Close the bucket lid and dispense the wipes as required.
  • Warnings

    • For external use only.
    • Store in cool and dry place.keep away from heat and direct sunlight.
    • Avoid touching eyes. In case of eye contact, flush thoroughly with water.
    • Avoid contact with broken skin.
    • Don't flush into toilet.
    • Stop use and ask a doctor if skin irritation develops.
  • KEEP OUT OF REACH OF CHILDREN

    • In case of accidental ingestion, seekprofessional assistance or contact a Poison Control Center immediately.
  • Directions

    • Thoroughly moisten the skin or solid surface with the product and let it dry without wiping
    • For children under 6, use only under adult supervision.
    • Not recommended for infants.
  • Inactive ingredients

    • Water, Glycerin
  • Package Label - Principal Display Panel

    53 mL NDC: 52489-001-01

    label-10-1label-10-2

    285 mL NDC: 52489-001-02

    label-60

    1020 mL NDC: 52489-001-03

    label-250

    3025 mL NDC: 52489-001-04

    label-800

    3.6 mL NDC: 52489-001-05

    label-1-1label-1-2

    4.8 mL NDC: 52489-001-06

    label-1-3label-1-4

    350 mL NDC: 52489-001-07

    label-80

    350 mL NDC: 52489-001-08

    label-100 pail

    135ml NDC:52489-001-09

    label-25 wipes package265ml NDC:52489-001-10

    label-50 wipes package535ml NDC:52489-001-11

    label-100 package

    720ml NDC:52489-001-12

    label-300 wipes pail2140ml NDC:52489-001-13

    label-500 wipes inner packagelabel-500 wipes external pail1910ml NDC:52489-001-14

    label-800

    4760ml NDC:52489-001-15

    label-2000 wipes pail7140ml NDC:52489-001-16

    label-3000 wipes pail

    280 mL NDC: 52489-001-17

    80pcs-280ml560 mL NDC: 52489-001-18

    160pcs-560ml

    1020 mL NDC: 52489-001-19

    label-250 package1label-250 package2

  • INGREDIENTS AND APPEARANCE
    SWEET CAREFOR ALCOHOL WIPES 
    alcohol cloth
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:52489-001
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL75 mL  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    GLYCERIN (UNII: PDC6A3C0OX)  
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:52489-001-0153 mL in 1 PACKAGE; Type 0: Not a Combination Product04/30/2020
    2NDC:52489-001-02285 mL in 1 PACKAGE; Type 0: Not a Combination Product04/30/2020
    3NDC:52489-001-031020 mL in 1 PAIL; Type 0: Not a Combination Product04/30/2020
    4NDC:52489-001-043025 mL in 1 PAIL; Type 0: Not a Combination Product04/30/2020
    5NDC:52489-001-053.6 mL in 1 PACKAGE; Type 0: Not a Combination Product05/22/2020
    6NDC:52489-001-064.8 mL in 1 PACKAGE; Type 0: Not a Combination Product05/22/2020
    7NDC:52489-001-07350 mL in 1 PACKAGE; Type 0: Not a Combination Product05/28/2020
    8NDC:52489-001-08350 mL in 1 PAIL; Type 0: Not a Combination Product05/28/2020
    9NDC:52489-001-09135 mL in 1 PACKAGE; Type 0: Not a Combination Product07/22/2020
    10NDC:52489-001-10265 mL in 1 PACKAGE; Type 0: Not a Combination Product07/22/2020
    11NDC:52489-001-11535 mL in 1 PACKAGE; Type 0: Not a Combination Product07/22/2020
    12NDC:52489-001-12720 mL in 1 PAIL; Type 0: Not a Combination Product07/22/2020
    13NDC:52489-001-132140 mL in 1 PAIL; Type 0: Not a Combination Product07/22/2020
    14NDC:52489-001-141910 mL in 1 PAIL; Type 0: Not a Combination Product07/22/2020
    15NDC:52489-001-154760 mL in 1 PAIL; Type 0: Not a Combination Product07/22/2020
    16NDC:52489-001-167140 mL in 1 PAIL; Type 0: Not a Combination Product07/22/2020
    17NDC:52489-001-17280 mL in 1 PAIL; Type 0: Not a Combination Product11/18/2020
    18NDC:52489-001-18560 mL in 1 PAIL; Type 0: Not a Combination Product11/18/2020
    19NDC:52489-001-191020 mL in 1 PACKAGE; Type 0: Not a Combination Product04/28/2021
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph Drug505G(a)(3)04/30/2020
    Labeler - Imperial Palace Commodity(shenzhen)CO.,LTD (527796368)
    Registrant - Imperial Palace Commodity(Dongguan)CO.,LTD (544367643)
    Establishment
    NameAddressID/FEIBusiness Operations
    Imperial Palace Commodity(Dongguan)CO.,LTD544367643manufacture(52489-001)
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