Label: HILL COUNTRY ESSENTIALS- triclosan liquid 

  • Label RSS
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: OTC monograph not final

NOTE: Most over the counter (OTC) are not reviewed and approved by the 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 01/13

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

  • ACTIVE INGREDIENT

    TRICLOSAN 0.15%

    PURPOSE

    ANTIBACTERIAL

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  • USES

    HELPS REDUCE BACTERIA ON THE SKIN.

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  • WARNINGS

    FOR EXTERNAL USE ONLY

    WHEN USING THIS PRODUCT

    AVOID CONTACT WITH EYES. IF CONTACT OCCURS, RINSE EYES WITH WATER.

    STOP USING THIS PRODUCT AND ASK DOCTOR IF

    IRRITATION OR REDNESS DEVELOP.

    KEEP OUT OF REACH OF CHILDREN

    IN CASE OF ACCIDENTAL INGESTION, GET MEDICAL HELP OR CONTACT A POISON CONTROL CENTER IMMEDIATELY.

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  • DIRECTIONS

    APPLY ONTO WET HANDS. WORK INTO A LATHER, RINSE THOROUGHLY.

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  • QUESTIONS/COMMENTS?

    1-866-695-3030

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  • INACTIVE INGREDIENTS

    WATER (AQUA), SODIUM C14-16 OLEFIN SULFONATE, LAURAMIDE DEA, SODIUM CHLORIDE, COCAMIDOPROPYL BETAINE, FRAGRANCE (PARFUM), CITRIC ACID, DMDM HYDANTOIN, GLYCERIN, TETRASODIUM EDTA, POLYQUATERNIUM-7, HYDROLYZED SILK, ALOE BARBADENSIS LEAF JUICE, RED 40 (CI 16035), YELLOW 5 (CI 19140), RED 33 (CI 17200).

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  • LABEL COPY
  • INGREDIENTS AND APPEARANCE
    HILL COUNTRY ESSENTIALS 
    triclosan liquid
    Product Information
    Product Type HUMAN OTC DRUG LABEL Item Code (Source) NDC:37808-215
    Route of Administration TOPICAL DEA Schedule     
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    TRICLOSAN (TRICLOSAN) TRICLOSAN 1.5 mg  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    WATER  
    SODIUM C14-16 OLEFIN SULFONATE  
    LAURIC DIETHANOLAMIDE  
    SODIUM CHLORIDE  
    COCAMIDOPROPYL BETAINE  
    CITRIC ACID MONOHYDRATE  
    DMDM HYDANTOIN  
    GLYCERIN  
    EDETATE SODIUM  
    POLYQUATERNIUM-7 (70/30 ACRYLAMIDE/DADMAC; 1600000 MW)  
    SILK, BASE HYDROLYZED (1000 MW)  
    ALOE VERA LEAF  
    FD&C RED NO. 40  
    FD&C YELLOW NO. 5  
    D&C RED NO. 33  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:37808-215-08 236 mL in 1 BOTTLE, PLASTIC
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    OTC monograph not final part333E 01/15/2013
    Labeler - H.E.B. (007924756)
    Registrant - APOLLO HEALTH AND BEAUTY CARE (201901209)
    Establishment
    Name Address ID/FEI Business Operations
    APOLLO HEALTH AND BEAUTY CARE 201901209 manufacture(37808-215)
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