Label: 8HD HAND AND SKIN SANITIZER- benzalkonium chloride liquid

  • NDC Code(s): 72513-200-01, 72513-200-02, 72513-200-03, 72513-200-04, view more
    72513-200-05, 72513-200-06, 72513-200-07
  • Packager: Strategia Project Management, Inc.
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated December 20, 2023

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

View All Sections
  • DRUG FACTS

  • ACTIVE INGREDIENT

    Benzalkonium Chloride 0.13%

    PURPOSE

    Antimicrobial

  • USES:

    Sanitizes hands and skin to help reduce bacteria that potentially cause diseases.

  • WARNINGS:

    For external use only.

    Do not use

    in eyes. If contact occurs, flush thoroughly with water.

    Stop use and ask a doctor:

    If irritation or redness develops, or if condition persists for more than 72 hours.

    Keep out of reach of children:

    If swallowed, get medical help or contact a Poison Control Center.

  • DIRECTIONS:

    On dry hands, place enough product in your palms to thoroughly cover the targeted area. Rub briskly until entirely dry.

  • Inactive Ingredients:

    Water, Hydrated Silica Complex

  • Package Labeling:72513-200-01

    1oz 72513-200-01

  • Package Labeling:72513-200-02

    2oz 72513-200-02

  • Package Labeling:72513-200-03

    1L 72513-200-03

  • Package Labeling:72513-200-04

    1Gal 72513-200-04

  • Package Labeling:72513-200-05

    55Gal 72513-200-05

  • Package Labeling:72513-200-06

    275Gal 72513-200-06

  • Package Labeling:72513-200-07

    330Gal 72513-200-07

  • INGREDIENTS AND APPEARANCE
    8HD HAND AND SKIN SANITIZER 
    benzalkonium chloride liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:72513-200
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE0.13 g  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    HYDRATED SILICA (UNII: Y6O7T4G8P9) 0.04 g  in 100 mL
    WATER (UNII: 059QF0KO0R) 99.83 g  in 100 mL
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:72513-200-0129.57 mL in 1 BOTTLE; Type 0: Not a Combination Product12/16/2020
    2NDC:72513-200-0259.14 mL in 1 BOTTLE; Type 0: Not a Combination Product12/16/2020
    3NDC:72513-200-031000 mL in 1 BOTTLE; Type 0: Not a Combination Product12/16/2020
    4NDC:72513-200-043785.41 mL in 1 JUG; Type 0: Not a Combination Product12/16/2020
    5NDC:72513-200-05208198 mL in 1 DRUM; Type 0: Not a Combination Product12/16/2020
    6NDC:72513-200-061040988.2 mL in 1 CONTAINER; Type 0: Not a Combination Product12/16/2020
    7NDC:72513-200-071249185.9 mL in 1 CONTAINER; Type 0: Not a Combination Product12/16/2020
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01612/16/2020
    Labeler - Strategia Project Management, Inc. (054047254)
View All Sections

Find additional resources

(also available in the left menu)

Safety

Report Adverse Events, FDA Safety Recalls, Presence in Breast Milk

Related Resources

Medline Plus, Clinical Trials, PubMed, Biochemical Data Summary

More Info on this Drug

View Labeling Archives, RxNorm, Get Label RSS Feed, View NDC Code(s)NEW!