Label: BCP HAND SANITIZER- alcohol gel

  • 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 June 12, 2020

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

  • ACTIVE INGREDIENTS

    ethanol alchol 65%

  • PURPOSE

    Antiseptic

  • INACTIVE INGREDIENT

    Water, Glycerin, Propylene glycol, Cabomer940, Aloe Vera gel, Triethanolamine, Jojoba Oil
    green tea Leaf Extract, Chamaecyparis Lawsoniana Wood Oil

  • USE

    Sanitizer to help reduce bacteria that potentially can cause disease. For use when soap and water are not available.

  • OTHER INFORMATION

    1. Store in cool and shady place, between 15-30C (59-86F)

    2. May discolor certain fabrics or surfaces.

  • Stop use and ask a doctor if sings symptoms as follows

    1) signs of irritation and/or rash appears

    (2) signs of abnormality as above after exposed to sunlight.

  • KEEP OUT OF REACH OF CHILDREN.

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

  • Do not use

    In children less than 2 months of age.
    On open skin wounds

  • WARNING

    Flammable. Keep away from heat or flame. Use only as intended and according to the directions of use.

  • When using this product

    keep out of eyes, ears, and mouth. In case of contact with eyes, rinse eyes thorough with water.

  • Directions

    Watch for children under 6 years of age to avoid rubbing, rubbing them on their backs, or drinking this product.

  • PAKAGE LABEL

    60ml 78252-301-01

    78252-301-01

    125ml 78252-301-02

    78252-301-02

    250ml 78252-301-03

    78252-301-03500ml 78252-301-04

    78252-301-04

    1000ml 78252-301-05

    78252-301-05

    200L 78252-301-06

    78252-301-06

    1000L 78252-301-07

    78252-301-07

  • INGREDIENTS AND APPEARANCE
    BCP HAND SANITIZER 
    alcohol gel
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:78252-301
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL65 mL  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R) 34.13 mL  in 100 mL
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3) 0.2 mL  in 100 mL
    CARBOMER 940 (UNII: 4Q93RCW27E) 0.2 mL  in 100 mL
    ALOE VERA LEAF (UNII: ZY81Z83H0X) 0.02 mL  in 100 mL
    JOJOBA OIL (UNII: 724GKU717M) 0.02 mL  in 100 mL
    GREEN TEA LEAF (UNII: W2ZU1RY8B0) 0.02 mL  in 100 mL
    CHAMAECYPARIS LAWSONIANA WOOD OIL (UNII: 0H3D02DVNU) 0.01 mL  in 100 mL
    GLYCERIN (UNII: PDC6A3C0OX) 0.2 mL  in 100 mL
    TROLAMINE (UNII: 9O3K93S3TK) 0.2 mL  in 100 mL
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:78252-301-0160 mL in 1 BOTTLE; Type 0: Not a Combination Product06/14/2020
    2NDC:78252-301-02125 mL in 1 BOTTLE; Type 0: Not a Combination Product06/14/2020
    3NDC:78252-301-03250 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product06/14/2020
    4NDC:78252-301-04500 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product06/14/2020
    5NDC:78252-301-051000 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product06/14/2020
    6NDC:78252-301-071000000 mL in 1 DRUM; Type 0: Not a Combination Product06/14/2020
    7NDC:78252-301-06200000 mL in 1 DRUM; Type 0: Not a Combination Product06/14/2020
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333A06/14/2020
    Labeler - Best Chance Products, LLC (117527140)
    Establishment
    NameAddressID/FEIBusiness Operations
    ECOSEM Co.,Ltd.695632865manufacture(78252-301)