Label: PROFESSIONAL THERAPY MUSCLECARE PRO- menthol and camphor cream
- NDC Code(s): 70039-303-04, 70039-303-16, 70039-303-32
- Packager: ACTIVE AND INNOVATIVE, LLC
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated May 3, 2024
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- Official Label (Printer Friendly)
- Active Ingredient (% by weight)
- Purpose
- Uses:
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Warnings:
For external use only.
- Caution: Discontinue use if excessive irritation of the skin develops. 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. Flammable: Keep away from fire and flame.
- Directions:
- Other Information:
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Inactive Ingredients:
Acacia Senegal Gum, Aloe Barbadensis Leaf Juice, Carthamus Tinctorius (Safflower) Oleosomes, Cetearyl Alcohol, Cetyl Alcohol, Chondroitin Sulfate, D-Glucosamine Sulfate Potassium, Dimethyl Sulfone (MSM), Ethylhexylglycerin, Eucalyptus Globulus Leaf/Twig Oil, Gaultheria Procumbens (Wintergreen) Leaf Oil, Glycerin, Magnesium Chloride, Phenoxyethanol, Polysorbate 60, Thymol, Tocopherol, Urea, Vitis Vinifera (Grape) Seed Oil, Water, Xanthan Gum
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INGREDIENTS AND APPEARANCE
PROFESSIONAL THERAPY MUSCLECARE PRO
menthol and camphor creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:70039-303 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 g in 100 g MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A) MENTHOL 4 g in 100 g Inactive Ingredients Ingredient Name Strength ACACIA (UNII: 5C5403N26O) ALOE VERA LEAF (UNII: ZY81Z83H0X) CARTHAMUS TINCTORIUS (SAFFLOWER) OLEOSOMES (UNII: 9S60Q72309) CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S) CETYL ALCOHOL (UNII: 936JST6JCN) CHONDROITIN SULFATE (BOVINE) (UNII: 6IC1M3OG5Z) GLUCOSAMINE SULFATE POTASSIUM CHLORIDE (UNII: 15VQ11I66N) DIMETHYL SULFONE (UNII: 9H4PO4Z4FT) ETHYLHEXYLGLYCERIN (UNII: 147D247K3P) EUCALYPTUS OIL (UNII: 2R04ONI662) METHYL SALICYLATE (UNII: LAV5U5022Y) GLYCERIN (UNII: PDC6A3C0OX) MAGNESIUM CHLORIDE (UNII: 02F3473H9O) PHENOXYETHANOL (UNII: HIE492ZZ3T) POLYSORBATE 60 (UNII: CAL22UVI4M) THYMOL (UNII: 3J50XA376E) TOCOPHEROL (UNII: R0ZB2556P8) UREA (UNII: 8W8T17847W) GRAPE SEED OIL (UNII: 930MLC8XGG) WATER (UNII: 059QF0KO0R) XANTHAN GUM (UNII: TTV12P4NEE) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:70039-303-32 906 g in 1 BOTTLE, PUMP; Type 0: Not a Combination Product 05/03/2024 2 NDC:70039-303-04 115 g in 1 TUBE; Type 0: Not a Combination Product 05/03/2024 3 NDC:70039-303-16 453 g in 1 BOTTLE, PUMP; Type 0: Not a Combination Product 05/03/2024 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M017 05/03/2024 Labeler - ACTIVE AND INNOVATIVE, LLC (206978079) Registrant - MCKENNA LABS, INC. (090631412) Establishment Name Address ID/FEI Business Operations MCKENNA LABS, INC. 090631412 manufacture(70039-303)