Label: HIGUYS- ethyl alcohol liquid

  • 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 May 28, 2020

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  • DRUG FACTS

  • ACTIVE INGREDIENTS:

    ETHYL ALCOHOL 75%

  • PURPOSE

    ANTISEPTIC

  • USES:

    HELPS REDUCE BACTERIA ON THE SKIN. RECOMMENDED FOR REPEATED USE.

  • WARNINGS: 

    FOR EXTERNAL USE ONLY. FLAMMABLE. KEEP AWAY FROM FIRE OR FLAME. WHEN USING THIS PRODUCT. AVOID CONTACT WITH EYES, IN CASE OF CONTACT WITH EYES, FLUSH THOROUGHLY WITH WATER. AVOID CONTACT WITH BROKEN SKIN. STOP USE AND ASK DOCTOR 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 RIGHT AWAY.

  • DIRECTIONS: 

    DISPENSE ONE PUMP OF SANITIZER ONTO HANDS AND RUB TOGETHER UNTIL DRY. USE AS NEEDED. FOR CHILDREN UNDER 6, USE WITH ADULT SUPERVISION. NOT RECOMMENDED FOR INFANTS.

  • OTHER INFO:

    STORE BELOW 1 Chuan (FAHREN DEGREES- HEIT). MAY CAUSE DISCOLORATION TO CERYAIN FABRICS AND SURFACES.

  • INACTIVE INGREDIENTS:

    WATER, CARBOMER, TRIETHANOLAMIN, ALOE EXTRACT, BELLIS PERENNIS EXTRACT, MORUS ALBA, RUBUS CHINGII, PUNICA GRANATUM, AVENA SATIVA

  • SPL UNCLASSIFIED SECTION

    Kills More Than 99.99% Of Germs

    ■ Use without water

    ■ Added moisturizer 

    SHIELD YOUR HANDS FROM GERMS & INFECTION NAYURALLY HIGUYS® PLANTBASED, SCENT FREE HAND SANITIZER, KEEPS YOUR HANDS CLEAN AND HYDRATED.

    HIGUYS®/WWW.LANCOUGROUP.COM

    CARA@LANCOUGROUP.COM

    CUSTOMER SERVICE: 0086 134 1624 1891

    MADE IN CHINA

  • Packaging

    image description

  • Packaging

    image description

  • INGREDIENTS AND APPEARANCE
    HIGUYS 
    ethyl alcohol liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:74416-170
    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
    WATER (UNII: 059QF0KO0R)  
    CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)  
    TROLAMINE (UNII: 9O3K93S3TK)  
    ALOE (UNII: V5VD430YW9)  
    BELLIS PERENNIS WHOLE (UNII: 2HU33I03UY)  
    MORUS ALBA WHOLE (UNII: C4228R0MX2)  
    RUBUS CHINGII WHOLE (UNII: A32A8VI76N)  
    PUNICA GRANATUM WHOLE (UNII: O2ZTS50U5E)  
    AVENA SATIVA FLOWERING TOP (UNII: MA9CQJ3F7F)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:74416-170-0153 mL in 1 BOTTLE; Type 0: Not a Combination Product05/14/2020
    2NDC:74416-170-0260 mL in 1 BOTTLE; Type 0: Not a Combination Product05/14/2020
    3NDC:74416-170-03100 mL in 1 BOTTLE; Type 0: Not a Combination Product05/14/2020
    4NDC:74416-170-04250 mL in 1 BOTTLE; Type 0: Not a Combination Product05/14/2020
    5NDC:74416-170-05300 mL in 1 BOTTLE; Type 0: Not a Combination Product05/14/2020
    6NDC:74416-170-06500 mL in 1 BOTTLE; Type 0: Not a Combination Product05/14/2020
    7NDC:74416-170-071000 mL in 1 BOTTLE; Type 0: Not a Combination Product05/14/2020
    8NDC:74416-170-085000 mL in 1 BOTTLE; Type 0: Not a Combination Product05/14/2020
    9NDC:74416-170-09236 mL in 1 BOTTLE; Type 0: Not a Combination Product05/14/2020
    10NDC:74416-170-104000 mL in 1 BOTTLE; Type 0: Not a Combination Product05/14/2020
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333A05/14/2020
    Labeler - Guangzhou C-kang Biotechnology Co., Ltd. (415992294)
    Establishment
    NameAddressID/FEIBusiness Operations
    Guangzhou C-kang Biotechnology Co., Ltd.415992294manufacture(74416-170)
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