Label: 75% ALCHOHOL INSTANT HAND SANITIZER gel

  • Contains inactivated NDC Code(s)
    NDC Code(s):     75242-005-01, 75242-005-02, 75242-005-03, 75242-005-04, view more
    75242-005-05, 75242-005-06, 75242-005-07, 75242-005-08, 75242-005-09, 75242-005-10, 75242-005-11, 75242-005-12, 75242-005-13, 75242-005-14, 75242-005-15
  • Packager: Cannapresso Health. Inc.
  • 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 April 14, 2020

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

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  • Active Ingredient(s)

    Isopropyl Alcohol 75% v/v. Purpose: Antiseptic

  • Purpose

    Antiseptic

  • Use

    TO DECREASE BACTERIA ON THE SKIN ,RECOMMENDED FOR REPEATED USE.

  • Warnings

    KEEP AWAY FROM FIRE OR FLAME.FOR EXTERNAL USE ONLY:HANDS

  • Do not use

    • in children less than 2 months of age
    • on open skin wounds
  • WHEN USING

    DO NOT USE IN OR NEAR IN OR HEAR THE EYES.IN CASE OF CONTACT,RINSE EYES THOROUGHLY WITH WATER.STOP USE AND ASK DOCTOR IF IRRITATION OR RASH APPEARS AND LASTS. KEEP OUT OF REACH FOR CHILDREN.

  • STOP USE

    Stop use and ask a doctor if irritation or rash occurs. These may be signs of a serious condition.

  • 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

    PLACE ENOUGH PRODUCT IN YOU PALM TO THOROUGHLY SPREAD ON BOTH HANDS AND RUB INTO THE SKIN UNTIL DRY.CHILDREN UNDER 6 YEARS OF AGE SHUOULD BE SUPERVISED WHEN USING THIS PRODUCT.

  • Other information

    STORE BELOW 41C.MAY DISCOLOR CERTAIN FABRICS OR SURFACES.

  • Inactive ingredients

    TROLAMINE,BERGAMOT OIL,CARBOMER 934,JOJOBA OIL,GLYCERIN,

    ALOE VERA LEAF,WATER,LEMON,VITAMIN E

  • Package Label - Principal Display Panel

    350ml60ml59ml499ml149ml200ml300ml100ml500ml119ml30ml250ml120ml349ml199ml

  • INGREDIENTS AND APPEARANCE
    75% ALCHOHOL INSTANT HAND SANITIZER 
    75% alchohol instant hand sanitizer gel
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:75242-005
    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
    LEMON (UNII: 24RS0A988O) 0.025 g  in 100 mL
    TROLAMINE (UNII: 9O3K93S3TK) 0.3 g  in 100 mL
    BERGAMOT OIL (UNII: 39W1PKE3JI) 0.025 g  in 100 mL
    CARBOMER 934 (UNII: Z135WT9208) 0.3 g  in 100 mL
    ALPHA-TOCOPHEROL (UNII: H4N855PNZ1) 0.02 g  in 100 mL
    GLYCERIN (UNII: PDC6A3C0OX) 5 mL  in 100 mL
    ALOE VERA LEAF (UNII: ZY81Z83H0X) 0.025 g  in 100 mL
    WATER (UNII: 059QF0KO0R)  
    JOJOBA OIL (UNII: 724GKU717M) 0.025 g  in 100 mL
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:75242-005-0130 mL in 1 BOTTLE; Type 0: Not a Combination Product04/15/2020
    2NDC:75242-005-0259 mL in 1 BOTTLE; Type 0: Not a Combination Product04/15/2020
    3NDC:75242-005-0360 mL in 1 BOTTLE; Type 0: Not a Combination Product04/15/2020
    4NDC:75242-005-04100 mL in 1 BOTTLE; Type 0: Not a Combination Product04/15/2020
    5NDC:75242-005-05119 mL in 1 BOTTLE; Type 0: Not a Combination Product04/15/2020
    6NDC:75242-005-06120 mL in 1 BOTTLE; Type 0: Not a Combination Product04/15/2020
    7NDC:75242-005-07149 mL in 1 BOTTLE; Type 0: Not a Combination Product04/15/2020
    8NDC:75242-005-08199 mL in 1 BOTTLE; Type 0: Not a Combination Product04/15/2020
    9NDC:75242-005-09200 mL in 1 BOTTLE; Type 0: Not a Combination Product04/15/2020
    10NDC:75242-005-10250 mL in 1 BOTTLE; Type 0: Not a Combination Product04/15/2020
    11NDC:75242-005-11300 mL in 1 BOTTLE; Type 0: Not a Combination Product04/15/2020
    12NDC:75242-005-12349 mL in 1 BOTTLE; Type 0: Not a Combination Product04/15/2020
    13NDC:75242-005-13350 mL in 1 BOTTLE; Type 0: Not a Combination Product04/15/2020
    14NDC:75242-005-14499 mL in 1 BOTTLE; Type 0: Not a Combination Product04/15/2020
    15NDC:75242-005-15500 mL in 1 BOTTLE; Type 0: Not a Combination Product04/15/2020
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333A04/15/2020
    Labeler - Cannapresso Health. Inc. (117477763)
    Establishment
    NameAddressID/FEIBusiness Operations
    Cannapresso Health. Inc.117477763manufacture(75242-005)
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