Label: WHOLE HEALTH HAND SANITIZERS 3-PACK- ethyl alcohol kit

  • 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 September 17, 2014

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

View All Sections
  • Active Ingredient

    Ethyl Alcohol 62%

  • Purpose

    Antiseptic

  • Uses

    Decreases bacteria on hands.

  • Warnings

    For external use only. Flammable, keep away from fire or flame.

  • When using this product

    do not get into eyes. If contact occurs, rinse thoroughly with water.

  • Stop use and ask a doctor

    if irritation or rash develops and continues for more than 72 hours.

  • Keep out of reach of children.

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

  • Directions

    Place a palmful of product in one hand. Spread on both hands and rub the skin until dry.

  • Inactive Ingredients

    Deionized water, Carbomer, Triethanolamine, Glycerin, D&C Violet 2, Fragrance

  • PRINCIPAL DISPLAY PANEL

    0.5FLOZ/15 ML

    MADE IN CHINA

    Expiration: 10/2016

  • Active Ingredient

    Ethyl Alcohol 62%

  • Purpose

    Antiseptic

  • Uses

    Decreases bacteria on hands.

  • Warnings

    For external use only. Flammable, keep away from fire or flame.

  • When using this product

    do not get into eyes. If contact occurs, rinse thoroughly with water.

  • Stop use and ask a doctor

     if irritation or rash develops and continues for more than 72 hours.

  • Keep out of reach of children.

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

  • Directions

    Place a palmful of product in one hand. Spread on both hands and rub the skin until dry.

  • Inactive Ingredients

    Deionized water, Carbomer, Triethanolamine, Glycerin, FD&C Green No. 3, Aloe, Fragrance.

  • SPL UNCLASSIFIED SECTION

    MADE IN CHINA

    Expiration: 10/2016

  • Active Ingredient

    Ethyl Alcohol 62%

  • Purpose

    Antiseptic

  • Uses

    Decreases bacteria on hands.

  • Warnings

    For external use only. Flammable, keep away from fire or flame.

  • When using this product

    do not get into eyes. If contact occurs, rinse thoroughly with water.

  • Stop use and ask a doctor

    if irritation or rash develops and continues for more than 72 hours.

  • Keep out of reach of children.

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

  • Directions

    Place a palmful of product in one hand. Spread on both hands and rub the skin until dry.

  • Inactive Ingredients

    Deionized water, Carbomer, Triethanolamine, Glycerin, Fragrance

  • PRINCIPAL DISPLAY PANEL

    whole health

    Instant
    Hand Sanitizer

    Kills Germs

    Lavender Scent

    0.5 FL OZ/15ML

  • PRINCIPAL DISPLAY PANEL

    whole health

    Instant Hand Sanitizer

    Kills Germs

    Aloe

    0.5 FL OZ/15ML

  • PRINCIPAL DISPLAY PANEL

    whole health

    Instant Hand Sanitizer

    Kills Germs

    Regular Scent

    0.5 FL OZ/15ML

  • PRINCIPAL DISPLAY PANEL

    HandSanitizer3pk

  • PRINCIPAL DISPLAY PANEL

    Fronts

  • PRINCIPAL DISPLAY PANEL

    Backs

  • INGREDIENTS AND APPEARANCE
    WHOLE HEALTH HAND SANITIZERS  3-PACK
    ethyl alcohol kit
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:69222-000
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:69222-000-001 in 1 KIT
    Quantity of Parts
    Part #Package QuantityTotal Product Quantity
    Part 11 BOTTLE 15 mL
    Part 21 BOTTLE 15 mL
    Part 31 BOTTLE 15 mL
    Part 1 of 3
    WHOLE HEALTH HAND SANITIZER  LAVENDER SCENT
    ethyl alcohol liquid
    Product Information
    Item Code (Source)NDC:69222-001
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL62 mL  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    TROLAMINE (UNII: 9O3K93S3TK)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    D&C VIOLET NO. 2 (UNII: 350KA7O6HK)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:69222-001-1515 mL in 1 BOTTLE
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333E09/17/2014
    Part 2 of 3
    WHOLE HEALTH HAND SANITIZER  ALOE
    ethyl alcohol liquid
    Product Information
    Item Code (Source)NDC:69222-002
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL62 mL  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    TROLAMINE (UNII: 9O3K93S3TK)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    FD&C GREEN NO. 3 (UNII: 3P3ONR6O1S)  
    ALOE (UNII: V5VD430YW9)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:69222-002-1515 mL in 1 BOTTLE
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333E09/17/2014
    Part 3 of 3
    WHOLE HEALTH HAND SANITIZER  REGULAR
    ethyl alcohol liquid
    Product Information
    Item Code (Source)NDC:69222-003
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL62 mL  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    TROLAMINE (UNII: 9O3K93S3TK)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:69222-003-1515 mL in 1 BOTTLE
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333E09/17/2014
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333E09/17/2014
    Labeler - Suzhou Jingying Daily Necessities Co., Ltd. (421370663)
    Establishment
    NameAddressID/FEIBusiness Operations
    Suzhou Jingying Daily Necessities Co., Ltd.421370663manufacture(69222-000)
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!