Label: SUPER WHITE STUFF PAIN RELIEF- menthol cream

  • NDC Code(s): 14448-307-50
  • Packager: BLUE SPRING WELLNESS, L.L.C.
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated November 10, 2023

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  • Drug Facts

  • Active Ingredient

    Menthol, USP 1.4%

    Purpose

    Topical Analgesic

  • Uses

    For the temporary relief of minor aches and pains associated with

    • arthritis
    • simple backahe
    • sprains
    • strains
    • bruises
  • Warnings:

    For external use only

    Do not use

    on wounded, damaged or irritated skin.

    When using this product

    • avoid contact with eyes or mucous membranes.
    • Do not bandage tightly

    Stop use and ask a doctor if

    • you experience a rash and/or a reaction 
    • condition worsens or if symptoms persist for more than 10 days or clears up and occur again within a few days.

    If Pregnant or Breast-Feeding 

    ask a health professional before use.

    Consult a doctor

    before use on children under 12 years of age if arthritis conditions are present. For all other listed uses, consult a doctor before use on children under 2 years of age.

    Keep out of reach of children.

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

  • Other information

    Store at room temperature.

  • Directions

    Apply to affected area not more than 3 to 4 times a days. before using for children under 12 for arthritic conditions and for all children under 2 years of age for all other uses. Consult a doctor

  • Inactive Ingrediets

    Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Aloe Barbadensis Leaf (Aloe Vera Gel) Juice, Anthemis Nobilis (Roman Chamomile) Oil, Aqua (Deionized Water), Arnica Montana Flower Extract, Ascorbyl Palmitate (Vitamin C), Calendula Officinalis Extract, Caprylyl Glycol, Centraurea Cyanus (Cornflower) Extract, Chamomilla Recutita (Chamomile) Extract, Chrysanthemum Parthenium (Feverfew) Extract, Coriandrum Sativum (Coriander) Oil, Emu Oil, Hamamelis Virginiana (Witch Hazel), Lamium Album (White Nettle) Extract, Methylsulfonylmethane (MSM), Phenoxyethanol, Salix Nigra (Willow) Bark Extract, Sodium Cocoyl Isethionate, Sodium Hydroxide, Sorbitol, Tetrasodium EDTA, Tilia Cordata (Linden) Extract, Tocopheryl Acetate (Vitamin E), Vitis Vinifera (Grape) Seed Extract.

  • Questions or Comments?

    Call or visit www.bluestuff.com 1-800-452-3700

  • Package Labeling:355

    Label3

  • INGREDIENTS AND APPEARANCE
    SUPER WHITE STUFF PAIN RELIEF 
    menthol cream
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:14448-307
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A) MENTHOL14 mg  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    ARNICA MONTANA FLOWER (UNII: OZ0E5Y15PZ)  
    ASCORBYL PALMITATE (UNII: QN83US2B0N)  
    CALENDULA OFFICINALIS FLOWER (UNII: P0M7O4Y7YD)  
    CAPRYLYL GLYCOL (UNII: 00YIU5438U)  
    CHAMOMILE (UNII: FGL3685T2X)  
    TANACETUM PARTHENIUM WHOLE (UNII: 6GE7Z0761K)  
    CORIANDER (UNII: 1OV56052IK)  
    EMU OIL (UNII: 344821WD61)  
    HAMAMELIS VIRGINIANA ROOT BARK/STEM BARK (UNII: T7S323PKJS)  
    LAMIUM ALBUM WHOLE (UNII: 046Y1357I6)  
    DIMETHYL SULFONE (UNII: 9H4PO4Z4FT)  
    PHENOXYETHANOL (UNII: HIE492ZZ3T)  
    SALIX NIGRA BARK (UNII: QU52J3A5B3)  
    SODIUM COCOYL ISETHIONATE (UNII: 518XTE8493)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    SORBITOL (UNII: 506T60A25R)  
    EDETATE SODIUM (UNII: MP1J8420LU)  
    TILIA CORDATA WHOLE (UNII: W5E5UB44GD)  
    .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
    VITIS VINIFERA SEED (UNII: C34U15ICXA)  
    CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED) (UNII: 59TL3WG5CO)  
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:14448-307-50335 mL in 1 BOTTLE; Type 0: Not a Combination Product08/01/2020
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01708/01/2020
    Labeler - BLUE SPRING WELLNESS, L.L.C. (182950118)
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