Label: SUPER WHITE STUFF PAIN RELIEF- menthol cream

  • NDC Code(s): 14448-315-00
  • Packager: BLUE SPRING WELLNESS, L.L.C.
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated November 10, 2023

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

  • Active Ingredient:

    Menthol, USP (1.4%)

    Purpose:

    Topical Analgesic

  • Uses:

    Temporary relief of minor aches and pains associsted with arthritis, simple backache, sprains, strains and 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 occurs again within a few days.

    If pregnant or breat-feeding 

    ask a health professional before use.

    Consult a doctor

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

    Keep out of reach of children.

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

  • Directions:

    Apply to affected area not more than 3 or 4 time a day.

  • Other Information:

    Store at room temperature.

  • Inactive Ingredients:

    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 Extarct.

  • Package Labeling:

    Label

  • INGREDIENTS AND APPEARANCE
    SUPER WHITE STUFF PAIN RELIEF 
    menthol cream
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:14448-315
    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
    CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED) (UNII: 59TL3WG5CO)  
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    CHAMAEMELUM NOBILE FLOWER OIL (UNII: UB27587839)  
    WATER (UNII: 059QF0KO0R)  
    ARNICA MONTANA FLOWER (UNII: OZ0E5Y15PZ)  
    ASCORBYL PALMITATE (UNII: QN83US2B0N)  
    CALENDULA OFFICINALIS FLOWER (UNII: P0M7O4Y7YD)  
    CAPRYLYL GLYCOL (UNII: 00YIU5438U)  
    CENTAUREA CYANUS FLOWER (UNII: QZ239038YC)  
    CHAMOMILE (UNII: FGL3685T2X)  
    TANACETUM PARTHENIUM WHOLE (UNII: 6GE7Z0761K)  
    CORIANDER OIL (UNII: 7626GC95E5)  
    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)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:14448-315-005 mL in 1 PACKET; Type 0: Not a Combination Product04/19/2021
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01704/19/2021
    Labeler - BLUE SPRING WELLNESS, L.L.C. (182950118)