Label: CAMPHOR, MENTHOL gel
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Contains inactivated NDC Code(s)
NDC Code(s): 50421-002-13 - Packager: Active & Innovative Inc.
- Category: HUMAN OTC DRUG LABEL
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 January 13, 2010
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- Official Label (Printer Friendly)
- Active Ingredients (% 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 the conditions worsens, or if the symptoms persists for more than 7 days or clears up and occurs 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.
- Directions
- Other Information
- Inactive Ingredients
- Questions?
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Principal Display Panel
PROFESSIONAL THERAPY EXTRA STRENGTH
EXTRA FUERTE
MuscleCare TM
PAIN RELIEVING GEL/ GEL ALIVIANTE DEL DOLOR
by/ por el Dr. Chris Oswald
FOR MUSCLE
& JOINT
PAIN
RELIEF
PARA EL
ALIVIO DEL
DOLOR
MUSCULAR Y
ARTICULAR
NET Wt. Peso. NETO
85g (3OZ.)
Distributed by: Muscle care products
1st. Clair Avenue East, Suite 1001,
Toronto, ON M4T 2V7
Professional Therapy Muscle Care TM
is a registered trademark of Active &
Innovative Inc.
MADE IN CANADA.
Tiene alguna pregunta? Llame al
415-967-3746
Distribuido por: Muscle care products
1st. Clair Avenue East, Suite 1001,
Toronto, ON M4T 2V7
Professional Therapy Muscle Care TM
es una marca registrada de Active &
Innovative Inc.
FABRICADO EN CANADA
www.muscleandback.com -
INGREDIENTS AND APPEARANCE
CAMPHOR, MENTHOL
camphor, menthol gelProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:50421-002 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength CAMPHOR (UNII: 5TJD82A1ET) (CAMPHOR - UNII:5TJD82A1ET) CAMPHOR 3.4 g in 85 g MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A) MENTHOL 8.5 g in 85 g Inactive Ingredients Ingredient Name Strength EUCALYPTUS OIL (UNII: 2R04ONI662) GLUCOSAMINE SULFATE (UNII: 1FW7WLR731) GLYCERIN (UNII: PDC6A3C0OX) MAGNESIUM CHLORIDE (UNII: 02F3473H9O) DIMETHYL SULFONE (UNII: 9H4PO4Z4FT) PEPPERMINT OIL (UNII: AV092KU4JH) PROPYLENE GLYCOL (UNII: 6DC9Q167V3) TROLAMINE (UNII: 9O3K93S3TK) WATER (UNII: 059QF0KO0R) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:50421-002-13 85 g in 1 BOTTLE, WITH APPLICATOR Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final part348 01/13/2010 Labeler - Active & Innovative Inc. (206978079) Establishment Name Address ID/FEI Business Operations International Laboratories (Canada) Ltd. 247010150 manufacture