Label: BLUESPRING DOCTORS PAIN FORMULA PAIN RELIEF- menthol cream

  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated July 14, 2025

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  • Product Facts

  • Active Ingredient

    Menthol, USP 1.4%

    Purpose

    Topical Analgesic

  • Uses

    For the temporary relief of minor aches and pains associated with • arthritis • simple backache • 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 clear up and occur again within few days.

    If Pregnant or Breast-Feeding

    ask a health professional before use. Consult a doctorbefore 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 or 4 times a day. Consult a doctorbefore using for children under 12 for arthritic conditions and for all children under 2 years of age for all other uses.
  • Inactive Ingredients

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

  • Questions or Comments?

    Call 1-855-290-7111or visit www.painrelief.md

  • Package Labeling:

    Label0

  • INGREDIENTS AND APPEARANCE
    BLUESPRING DOCTORS PAIN FORMULA PAIN RELIEF 
    menthol cream
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:83591-629
    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
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    WATER (UNII: 059QF0KO0R)  
    ARGAN OIL (UNII: 4V59G5UW9X)  
    ARNICA MONTANA FLOWER (UNII: OZ0E5Y15PZ)  
    ASCORBYL PALMITATE (UNII: QN83US2B0N)  
    CALENDULA OFFICINALIS FLOWER (UNII: P0M7O4Y7YD)  
    CAPRYLYL GLYCOL (UNII: 00YIU5438U)  
    CHAMOMILE (UNII: FGL3685T2X)  
    CORIANDER (UNII: 1OV56052IK)  
    EMU OIL (UNII: 344821WD61)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    WITCH HAZEL (UNII: 101I4J0U34)  
    DIMETHYL SULFONE (UNII: 9H4PO4Z4FT)  
    PHENOXYETHANOL (UNII: HIE492ZZ3T)  
    SALIX NIGRA BARK (UNII: QU52J3A5B3)  
    SODIUM COCOYL ISETHIONATE (UNII: 518XTE8493)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    SORBITOL (UNII: 506T60A25R)  
    FEVERFEW (UNII: Z64FK7P217)  
    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:83591-629-00355 mL in 1 JAR; Type 0: Not a Combination Product07/07/2025
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01707/07/2025
    Labeler - ACA MANAGEMENT LLC (119034214)
    Registrant - Pure Source, LLC (080354456)
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