Label: ALCOHOL WIPES- alcohol cloth

  • Contains inactivated NDC Code(s)
    NDC Code(s):
    75749-051-01, 75749-051-02, 75749-051-03, 75749-051-04, view more
    75749-051-05, 75749-051-06, 75749-051-07, 75749-051-08, 75749-051-09, 75749-051-10, 75749-051-11, 75749-051-12, 75749-051-13, 75749-051-14, 75749-051-15, 75749-051-16, 75749-051-17, 75749-051-18, 75749-051-19, 75749-051-20
  • Packager: Ningbo Pretty Tourism Manufacture Co., Ltd
  • 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 August 11, 2020

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

  • Active Ingredient

    Ethyl Alcohol 75%

  • Purpose

    Anitbacterial

  • Use

    decrease bacteria on skin

  • Warnings

    For external use only.

    Do not use

    If you are allergic to any of the ingredients

    When using this product

    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

    Stop use and ask a doctor if irritation or rash occurs develops and continues for more than 72 hours

    Keep out of reach of children

    Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

  • Directions

    adult and children 2years and over

    • apply to hands
    • allow to dry without wiping

    children under 2 years

    • ask a doctor before use
  • Inactive ingredients

    Water

    Glycerin

    Aloe barbadensis extract

  • Package Label - Principal Display Panel

    Label

  • INGREDIENTS AND APPEARANCE
    ALCOHOL WIPES 
    alcohol cloth
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:75749-051
    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)  
    ALOE (UNII: V5VD430YW9)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:75749-051-011 in 1 CONTAINER08/11/2020
    15 mL in 1 CONTAINER; Type 0: Not a Combination Product
    2NDC:75749-051-022 in 1 CONTAINER08/11/2020
    210 mL in 1 CONTAINER; Type 0: Not a Combination Product
    3NDC:75749-051-0310 in 1 CONTAINER08/11/2020
    31 in 1 CONTAINER
    35 mL in 1 CONTAINER; Type 0: Not a Combination Product
    4NDC:75749-051-0412 in 1 CONTAINER08/11/2020
    41 in 1 CONTAINER
    45 mL in 1 CONTAINER; Type 0: Not a Combination Product
    5NDC:75749-051-0520 in 1 CONTAINER08/11/2020
    51 in 1 CONTAINER
    55 mL in 1 CONTAINER; Type 0: Not a Combination Product
    6NDC:75749-051-0624 in 1 CONTAINER08/11/2020
    61 in 1 CONTAINER
    65 mL in 1 CONTAINER; Type 0: Not a Combination Product
    7NDC:75749-051-0730 in 1 CONTAINER08/11/2020
    71 in 1 CONTAINER
    75 mL in 1 CONTAINER; Type 0: Not a Combination Product
    8NDC:75749-051-0840 in 1 CONTAINER08/11/2020
    81 in 1 CONTAINER
    85 mL in 1 CONTAINER; Type 0: Not a Combination Product
    9NDC:75749-051-0948 in 1 CONTAINER08/11/2020
    91 in 1 CONTAINER
    95 mL in 1 CONTAINER; Type 0: Not a Combination Product
    10NDC:75749-051-1050 in 1 CONTAINER08/11/2020
    101 in 1 CONTAINER
    105 mL in 1 CONTAINER; Type 0: Not a Combination Product
    11NDC:75749-051-11100 in 1 CONTAINER08/11/2020
    111 in 1 CONTAINER
    115 mL in 1 CONTAINER; Type 0: Not a Combination Product
    12NDC:75749-051-1210 in 1 CONTAINER08/11/2020
    122 in 1 CONTAINER
    1210 mL in 1 CONTAINER; Type 0: Not a Combination Product
    13NDC:75749-051-1312 in 1 CONTAINER08/11/2020
    132 in 1 CONTAINER
    1310 mL in 1 CONTAINER; Type 0: Not a Combination Product
    14NDC:75749-051-1420 in 1 CONTAINER08/11/2020
    142 in 1 CONTAINER
    1410 mL in 1 CONTAINER; Type 0: Not a Combination Product
    15NDC:75749-051-1524 in 1 CONTAINER08/11/2020
    152 in 1 CONTAINER
    1510 mL in 1 CONTAINER; Type 0: Not a Combination Product
    16NDC:75749-051-1630 in 1 CONTAINER08/11/2020
    162 in 1 CONTAINER
    1610 mL in 1 CONTAINER; Type 0: Not a Combination Product
    17NDC:75749-051-1740 in 1 CONTAINER08/11/2020
    172 in 1 CONTAINER
    1710 mL in 1 CONTAINER; Type 0: Not a Combination Product
    18NDC:75749-051-1848 in 1 CONTAINER08/11/2020
    182 in 1 CONTAINER
    1810 mL in 1 CONTAINER; Type 0: Not a Combination Product
    19NDC:75749-051-1950 in 1 CONTAINER08/11/2020
    192 in 1 CONTAINER
    1910 mL in 1 CONTAINER; Type 0: Not a Combination Product
    20NDC:75749-051-20100 in 1 CONTAINER08/11/2020
    202 in 1 CONTAINER
    2010 mL in 1 CONTAINER; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333A08/11/2020
    Labeler - Ningbo Pretty Tourism Manufacture Co., Ltd (553193489)
    Establishment
    NameAddressID/FEIBusiness Operations
    Ningbo Pretty Tourism Manufacture Co., Ltd553193489manufacture(75749-051)