Label: N-LABS SOLAR MAX TOPICAL ANALGESIC- menthol, capsaicin cream

  • NDC Code(s): 71856-271-00
  • Packager: NUTRIOMO LABS PTE. LTD.
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated November 5, 2023

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  • Drug Facts

  • Active ingredients

    Menthol 8% Capsaicin 0.025%

    Purpose

    Topical Analgesic

  • Uses

    For the temporary relief of minor aches and pains of muscles and joints associated with:

    ● simple backache ● arthritis ● strains ● bruises ● sprains

  • Warnings

    For external use only. Use only as directed.

    Do not use

    ● on wounds, damaged, or irritated skin ● with a heating pad ● if you are allergic to capsicum or chili peppers

    When using this product

    ● avoid contact with the eyes or mucous membranes ● do not bandage tightly ● a transient burning sensation may occur upon application but generally disappears in several days ● do not expose the treated area to heat or direct sunlight ● do not have water contact on area of skin where product is applied as this may cause a “burning” sensation due to the active ingredients in the product

    Stop use and ask a doctor if

    ● condition worsens, or if symptoms persist for more than 7 days or clear up and occur again within a few days ● redness is present or irritation develops ● a severe burning sensation occurs

    If pregnant or breast-feeding,

    ask a healthcare provider before use.

    Keep out of reach of children.

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

  • Directions

    ● use only as directed ● shake well before each use ● with the roller facing down, roll ball against skin to apply a thin layer of product to affected area ● massage gently into skin ● wait 30 minutes before reapplying consult a doctor Adults and children 18 years of age and older:Children under 18 years of age:

  • Other Information

    ● Store at room temperature 20-25°C (68-77°F).  ● Do not use if printed safety seal on cap is broken or missing” to keep the consistency.

  • Inactive Ingredients

    Aloe Barbadensis Leaf (Aloe Vera Gel) Juice, Angelica Archangelica Extract, Aqua (Deionized Water), Arnica Montana Flower Extract, Boswellia Serrata Extract, Calendula Officinalis Extract, Camellia Sinensis (Green Tea) Extract, Carbomer, Centella Asiatica (Gotu Kola) Extract, Chamomilla Matricaria (Chamomile) Extract, Ethylhexylglycerin, Eucalyptus Globulus Oil, Glycerin, llex Paraguariensis (Yerba Mate') Extract, Methylsulfonylmethane (MSM), Phenoxyethanol, Polysorbate-20, SD-Alcohol 40B, Sodium Lauryl Sulfate, Triethanolamine

  • Questions?

    Call us at 1-800-856-5587

  • Package Labeling:

    Label00

  • INGREDIENTS AND APPEARANCE
    N-LABS SOLAR MAX TOPICAL ANALGESIC 
    menthol, capsaicin cream
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:71856-271
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A) MENTHOL80 mg  in 1 mL
    CAPSAICIN (UNII: S07O44R1ZM) (CAPSAICIN - UNII:S07O44R1ZM) CAPSAICIN0.25 mg  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    WATER (UNII: 059QF0KO0R)  
    ARNICA MONTANA FLOWER (UNII: OZ0E5Y15PZ)  
    INDIAN FRANKINCENSE (UNII: 4PW41QCO2M)  
    CALENDULA OFFICINALIS FLOWER (UNII: P0M7O4Y7YD)  
    GREEN TEA LEAF (UNII: W2ZU1RY8B0)  
    CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)  
    CENTELLA ASIATICA TRITERPENOIDS (UNII: 4YS74Q4G4J)  
    CHAMOMILE (UNII: FGL3685T2X)  
    ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)  
    EUCALYPTUS OIL (UNII: 2R04ONI662)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    ILEX PARAGUARIENSIS LEAF (UNII: 1Q953B4O4F)  
    DIMETHYL SULFONE (UNII: 9H4PO4Z4FT)  
    PHENOXYETHANOL (UNII: HIE492ZZ3T)  
    POLYSORBATE 20 (UNII: 7T1F30V5YH)  
    SODIUM LAURYL SULFATE (UNII: 368GB5141J)  
    TROLAMINE (UNII: 9O3K93S3TK)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:71856-271-001 in 1 BOX02/01/2022
    160 mL in 1 TUBE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01702/01/2022
    Labeler - NUTRIOMO LABS PTE. LTD. (659264720)
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