Label: NICK RELIEF- aluminum sulfate stick

  • Category: HUMAN OTC DRUG LABEL

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 March 4, 2010

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  • BOXED WARNING (What is this?)

    Warnings: For external use only. Flammable product.
    Do not use in or around eyes or sensitive areas.
    Discontinue use and consult a doctor if bleeding persists.
    NICK RELIEF CARTON ARTWORK

  • DOSAGE & ADMINISTRATION

    Directions:
    Apply cold water to area and pat dry.
    Shake Nick Relief.
    Apply gently to area.
    Rinse applicator head with warm water after each use.
  • INDICATIONS & USAGE

    Uses:
    Stops bleeding from minor nicks and cuts.
    No stinging or skin irritation.
    Helps to speed healing.
  • ACTIVE INGREDIENT

    Active Ingredient: Aluminum Sulfate 46%
  • INACTIVE INGREDIENT

    Inactive ingredients: Witch Hazel Distillate, Water (Aqua), Propylene Glycol, Panthenol, Horsetail (Equisetum Arvense) Extract, Passionflower (Passiflora Incarnata) Fruit Extract, Diazolidinyl Urea, Methylparaben, Propylparaben
  • KEEP OUT OF REACH OF CHILDREN

    KEEP OUT OF REACH OF CHILDREN
  • PURPOSE

    Purpose: Stops bleeding
  • PRINCIPAL DISPLAY PANEL

    Clubman

    Nick Relief

    For razor nicks and cuts

    Stops Bleeding Instantly

    STICK ARTWORK

  • INGREDIENTS AND APPEARANCE
    NICK RELIEF 
    aluminum sulfate stick
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:57367-007
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALUMINUM SULFATE (UNII: 34S289N54E) (ALUMINUM CATION - UNII:3XHB1D032B) ALUMINUM SULFATE46 mg  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    WITCH HAZEL (UNII: 101I4J0U34)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    DIAZOLIDINYLUREA (UNII: H5RIZ3MPW4)  
    PANTHENOL (UNII: WV9CM0O67Z)  
    METHYLPARABEN (UNII: A2I8C7HI9T)  
    PROPYLPARABEN (UNII: Z8IX2SC1OH)  
    MELISSA OFFICINALIS (UNII: YF70189L0N)  
    MATRICARIA RECUTITA (UNII: G0R4UBI2ZZ)  
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    GERANIUM EXTRACT (UNII: 6H429I0Y3L)  
    QUERCUS ALBA (UNII: XR6BC2ZUAM)  
    ROSA CANINA FRUIT (UNII: 3TNW8D08V3)  
    SAGE (UNII: 065C5D077J)  
    COMFREY (UNII: D05HXK6R3G)  
    YARROW FLOWER (UNII: YQR8R0SQEA)  
    EAST INDIAN LEMONGRASS OIL (UNII: UP0M8M3VZW)  
    .ALPHA.-TOCOPHEROL ACETATE, D- (UNII: A7E6112E4N)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:57367-007-201 in 1 BLISTER PACK
    1NDC:57367-007-077 mL in 1 APPLICATOR
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph finalpart34711/27/1997
    Labeler - 220 LABORATORIES INC (783247950)
    Registrant - 220 LABORATORIES INC (783247950)
    Establishment
    NameAddressID/FEIBusiness Operations
    220 LABORATORIES INC783247950manufacture
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