Label: NICK RELIEF - aluminum sulfate stick

  • NDC Code(s): 57367-007-07, 57367-007-20
  • Packager: 220 LABORATORIES INC
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: OTC monograph 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 March 4, 2010

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

  • 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

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  • 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.
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  • INDICATIONS & USAGE

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

    Active Ingredient: Aluminum Sulfate 46%
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  • 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
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  • KEEP OUT OF REACH OF CHILDREN

    KEEP OUT OF REACH OF CHILDREN
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  • PURPOSE

    Purpose: Stops bleeding Close
  • PRINCIPAL DISPLAY PANEL

    Clubman

    Nick Relief

    For razor nicks and cuts

    Stops Bleeding Instantly

    STICK ARTWORK

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  • INGREDIENTS AND APPEARANCE
    NICK RELIEF 
    aluminum sulfate stick
    Product Information
    Product Type HUMAN OTC DRUG Item Code (Source) NDC:57367-007
    Route of Administration TOPICAL
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    ALUMINUM SULFATE (UNII: 34S289N54E) (ALUMINUM CATION - UNII:3XHB1D032B) ALUMINUM SULFATE 46 mg  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    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 Code Package Description Marketing Start Date Marketing End Date
    1 NDC:57367-007-20 1 in 1 BLISTER PACK
    1 NDC:57367-007-07 7 mL in 1 APPLICATOR
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    OTC monograph final part347 11/27/1997
    Labeler - 220 LABORATORIES INC (783247950)
    Registrant - 220 LABORATORIES INC (783247950)
    Establishment
    Name Address ID/FEI Business Operations
    220 LABORATORIES INC 783247950 manufacture
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