Professional Therapy MuscleCare Pain Relieving
- Dosage form
- OINTMENT
- Labeler
- Active and Innovative Inc.
- Label updated
- 2025-01-23
- Retrieved
- 2026-09-07
- Active ingredients
- CAMPHOR (SYNTHETIC) · MENTHOL
성분·작용
For muscle and joint pain relief
ACTIVE INGREDIENTS (% BY WEIGHT) PURPOSE
Menthol 4.0%...........................Analgesic (pain relief)
Camphor 4.0%........................Analgesic (pain relief)
USE:
For the temporary relief of minor aches and pains of muscles and joints associated with simple backache, arthritis, strains, bruises and sprains, etc.
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:
Use only as directed.
Do not use if you are pregnant or breastfeeding.
If swallowed, get medical help or contact a Poison Control center right away.
복용법·사용법
Directions: Adults and children 12 years of age or older: Rub this soothing cream onto the effected area not more than 3 to 4 times daily. Children under the age of 12: Do not use, consult a doctor.
보관·기타 정보
Other Information: Store under normal storage conditions. Store away from children.
첨가제
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
[Image in the official label — see DailyMed source]
DailyMed Set ID: 42f1abeb-f6d7-01c3-e054-00144ff88e88 · Version 3
NDC: 70039-300