Label: PROFESSIONAL THERAPY MUSCLECARE- diabetic pain relieving ointment
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Contains inactivated NDC Code(s)
NDC Code(s): 24488-027-30 - Packager: Active and Innovative
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: OTC monograph final
DISCLAIMER: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.
Drug Label Information
Updated June 2, 2011
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- Active Ingredients (% by weight)
- Purpose
- Uses:
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Warnings:
For external use only.
- Avoid getting into eyes or on mucous membranes.
- If condition worsens, or if symptoms persist for more than 7 days or clear up and occur again within a few days, discontinue use of this product and consult a doctor.
- Do not apply to wounds or damaged skin. Do not bandage tightly.
- Keep out of reach of children.
- Directions:
- Other Information:
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Inactive Ingredients:
Water/Aqua; Cetyl Alcohol, Glycol Stearate, MSM (Methylsulfonylmethane), Glycerin, Stearyl Alcohol, Glucosamine Sulfate, Polyacrylamide (and) C13-14 Isoparaffin (and) Laureth-7, Tocopheryl (Vitamain E) Acetate, Oil of Wintergreen (Methyl Salicylate), Cucumaria (Sea Cucumber) Frondosa, Grape Seed Oil, Urea, Phenoxyethanol (and) Caprylyl Glycol (and) Sorbic Acid, Polysorbate-20, Eucalyptus Globulus Leaf Oil, Thymol, Aloe Barbadensis Leaf Juice, Chondroitin Sulfate, Magnesium Chloride
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INGREDIENTS AND APPEARANCE
PROFESSIONAL THERAPY MUSCLECARE
diabetic pain relieving ointmentProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:24488-027 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength CAMPHOR (SYNTHETIC) (UNII: 5TJD82A1ET) (CAMPHOR (SYNTHETIC) - UNII:5TJD82A1ET) CAMPHOR (SYNTHETIC) 4.6 g in 115 g MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A) MENTHOL 4.6 g in 115 g Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) CETYL ALCOHOL (UNII: 936JST6JCN) GLYCOL STEARATE (UNII: 0324G66D0E) DIMETHYL SULFONE (UNII: 9H4PO4Z4FT) GLYCERIN (UNII: PDC6A3C0OX) STEARYL ALCOHOL (UNII: 2KR89I4H1Y) GLUCOSAMINE SULFATE (UNII: 1FW7WLR731) ACRYLAMIDE (UNII: 20R035KLCI) C13-14 ISOPARAFFIN (UNII: E4F12ROE70) LAURETH-7 (UNII: Z95S6G8201) ALPHA-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) METHYL SALICYLATE (UNII: LAV5U5022Y) CUCUMARIA FRONDOSA (UNII: 4M1271AZ6G) GRAPE SEED OIL (UNII: 930MLC8XGG) UREA (UNII: 8W8T17847W) PHENOXYETHANOL (UNII: HIE492ZZ3T) SORBIC ACID (UNII: X045WJ989B) POLYSORBATE 20 (UNII: 7T1F30V5YH) EUCALYPTUS OIL (UNII: 2R04ONI662) THYMOL (UNII: 3J50XA376E) ALOE VERA LEAF (UNII: ZY81Z83H0X) SULFATE ION (UNII: 7IS9N8KPMG) MAGNESIUM CHLORIDE (UNII: 02F3473H9O) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:24488-027-30 115 g in 1 TUBE Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final part341 06/02/2011 Labeler - Active and Innovative (961956229) Registrant - Creations Garden Natural Products (961956229) Establishment Name Address ID/FEI Business Operations Creations Garden Natural Products 961956229 manufacture