Label: DZUL ARTHRITIS PAIN RELIEF- menthol cream
- NDC Code(s): 83037-015-04
- Packager: Caball Sales, Inc.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated April 8, 2024
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- Official Label (Printer Friendly)
- ACTIVE INGREDIENT
- PURPOSE
- USE
- WARNINGS
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WHEN USING
Avoid contact with the eyes or mucous membranes.
Do not apply to wounds or damaged skin.
Do not apply to the irritated skin or if excessive irritation develops.
Do not bandage tightly.
Do not use with heating pad or device.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.
- PREGNANCY OR BREAST FEEDING
- KEEP OUT OF REACH OF CHILDREN
- DIRECTIONS
- OTHER INFORMATION
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INACTIVE INGREDIENT
Water (Aqua), Paraffinum Liquidum, Alcohol Denat, Cetearyl Alcohol, Cetyl Alcohol, Stearic Acid, Dimethicone, Glyceryl Stearate, Eucalyptus Globulus Leaf Oil, Glycereth-26, Polysorbate 60, Methylsulfonylmethane (MSM), Sodium Chondroitin Sulfate, Glucosamine Sulfate, Sodium Hyaluronate, Sodium PCA, Wheat Amino Acids, Panthenol, Symphytum Officinale (Comfrey) Extract, Hydroxyproline, Acrylamide/Sodium Acrylate Copolymer, Trideceth-6, Stearyl Alcohol, Polysorbate 20, Caprylyl Glycol, Sodium Hydroxide, Phenoxyethanol, Hexylene Glycol.
- DZUL ARTHRITIS PAIN RELIEF CREAM
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INGREDIENTS AND APPEARANCE
DZUL ARTHRITIS PAIN RELIEF
menthol creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:83037-015 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength MENTHOL, UNSPECIFIED FORM (UNII: L7T10EIP3A) (MENTHOL, UNSPECIFIED FORM - UNII:L7T10EIP3A) MENTHOL, UNSPECIFIED FORM 1.5 g in 100 g Inactive Ingredients Ingredient Name Strength EUCALYPTUS OIL (UNII: 2R04ONI662) POLYSORBATE 60 (UNII: CAL22UVI4M) DIMETHYL SULFONE (UNII: 9H4PO4Z4FT) MINERAL OIL (UNII: T5L8T28FGP) GLYCERYL STEARATE SE (UNII: FCZ5MH785I) ACRYLIC ACID/SODIUM ACRYLATE COPOLYMER (1:1; 600 MPA.S AT 0.2%) (UNII: M4PPW69Y4H) AMINO ACIDS, WHEAT (UNII: 0370GZL32F) PANTHENOL (UNII: WV9CM0O67Z) ALCOHOL (UNII: 3K9958V90M) STEARIC ACID (UNII: 4ELV7Z65AP) CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S) CETYL ALCOHOL (UNII: 936JST6JCN) DIMETHICONE (UNII: 92RU3N3Y1O) GLYCERETH-26 (UNII: NNE56F2N14) SODIUM CHONDROITIN SULFATE (PORCINE; 5500 MW) (UNII: H5BJH23Z9A) GLUCOSAMINE SULFATE (UNII: 1FW7WLR731) CAPRYLYL GLYCOL (UNII: 00YIU5438U) SODIUM HYDROXIDE (UNII: 55X04QC32I) SYMPHYTUM OFFICINALE WHOLE (UNII: H8FJJ6KX5Y) HYDROXYPROLINE (UNII: RMB44WO89X) STEARYL ALCOHOL (UNII: 2KR89I4H1Y) TRIDECETH-6 (UNII: 3T5PCR2H0C) HYALURONATE SODIUM (UNII: YSE9PPT4TH) SODIUM PYRROLIDONE CARBOXYLATE (UNII: 469OTG57A2) PHENOXYETHANOL (UNII: HIE492ZZ3T) HEXYLENE GLYCOL (UNII: KEH0A3F75J) POLYSORBATE 20 (UNII: 7T1F30V5YH) WATER (UNII: 059QF0KO0R) Product Characteristics Color white Score Shape Size Flavor Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:83037-015-04 114 g in 1 JAR; Type 0: Not a Combination Product 04/20/2024 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M017 04/20/2024 Labeler - Caball Sales, Inc. (047422138)