Label: PROFESSIONAL THERAPY MUSCLECARE PAIN RELIEVING- menthol, camphor ointment
- NDC Code(s): 70039-300-02
- Packager: Active and Innovative Inc.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: OTC monograph not 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 August 3, 2021
If you are a consumer or patient please visit this version.
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- Official Label (Printer Friendly)
- PURPOSE
- ACTIVE INGREDIENTS (% BY WEIGHT) PURPOSE
- USE:
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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:
- DOSAGE & ADMINISTRATION
- STORAGE AND HANDLING
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INACTIVE INGREDIENT
Inactive Ingredients:Dimethyl sulfone (MSM), Gluosamine sulfate, Tocopherol (natural Vitamin E), Safflower Oleosomes (Carthamus Tinctorius), Wintergreen leaf oil (Gaultheria fragrantissima Wall), Eucalyptus leaf oil 9Eucalyptus globus), Grape seed oil (Vitis vinifera), Aloe babadensis leaf juice, Thymol crystals (5-methyl-2-(1-methylethyl)phenol), Chondroitin sulfate, Cetyl alcohol, Cetearyl alcohol & Polysorbate-20, Glycerin, Acacia Senegal Gum & Xanthan Gum, Urea, Phenoxyethanol & ethylhexyl glycerin, Water, Magnesium chloride.
- Professional Therapy MuscleCare Pain Relieving Ointment by Dr. Chris Oswald
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INGREDIENTS AND APPEARANCE
PROFESSIONAL THERAPY MUSCLECARE PAIN RELIEVING
menthol, camphor ointmentProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:70039-300 Route of Administration CUTANEOUS, TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A) MENTHOL 40 mg in 1 g CAMPHOR (SYNTHETIC) (UNII: 5TJD82A1ET) (CAMPHOR (SYNTHETIC) - UNII:5TJD82A1ET) CAMPHOR (SYNTHETIC) 40 mg in 1 g Inactive Ingredients Ingredient Name Strength DIMETHYL SULFONE (UNII: 9H4PO4Z4FT) GLUCOSAMINE SULFATE (UNII: 1FW7WLR731) METHYL SALICYLATE (UNII: LAV5U5022Y) EUCALYPTUS OIL (UNII: 2R04ONI662) ALOE VERA LEAF (UNII: ZY81Z83H0X) THYMOL (UNII: 3J50XA376E) XANTHAN GUM (UNII: TTV12P4NEE) UREA (UNII: 8W8T17847W) PHENOXYETHANOL (UNII: HIE492ZZ3T) ACACIA (UNII: 5C5403N26O) GRAPE SEED OIL (UNII: 930MLC8XGG) TOCOPHEROL (UNII: R0ZB2556P8) CARTHAMUS TINCTORIUS (SAFFLOWER) OLEOSOMES (UNII: 9S60Q72309) CHONDROITIN SULFATE (CHICKEN) (UNII: 7VZ9466BAB) CETYL ALCOHOL (UNII: 936JST6JCN) CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S) POLYSORBATE 20 (UNII: 7T1F30V5YH) GLYCERIN (UNII: PDC6A3C0OX) ETHYLHEXYLGLYCERIN (UNII: 147D247K3P) WATER (UNII: 059QF0KO0R) MAGNESIUM CHLORIDE (UNII: 02F3473H9O) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:70039-300-02 115 g in 1 TUBE; Type 0: Not a Combination Product 01/01/2017 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part348 01/01/2017 Labeler - Active and Innovative Inc. (206978079) Establishment Name Address ID/FEI Business Operations Delta Pharma Inc. 200161730 manufacture(70039-300) Establishment Name Address ID/FEI Business Operations PureTek Corporation 785961046 manufacture(70039-300)
