FDA Label for Dch Arthritis Relief
View Indications, Usage & Precautions
Dch Arthritis Relief Product Label
The following document was submitted to the FDA by the labeler of this product Derma Care Research Labs, Llc. The document includes published materials associated whith this product with the essential scientific information about this product as well as other prescribing information. Product labels may durg indications and usage, generic names, contraindications, active ingredients, strength dosage, routes of administration, appearance, warnings, inactive ingredients, etc.
Otc - Active Ingredient
Trolamine Salicylate 10%
Otc - Purpose
Topical Analgesic.
Dosage & Administration
Temporarily relieves minor pain associated with arthritis, simple backache, muscle strains, sprains, and cramps.
Warnings
For external use only.
Allergy Alert: if prone to allergic reaction from aspirin or salicylates, consult a doctor before use.
When using this product use only as directed, avoid taking a bath or shower within 1 hour before or after applying, do not bandage or use with a heating pad, avoid contact with eyes or mucous membranes, do not apply to wounds or damaged skin.
Stop use and ask a doctor if condition worsens or symptoms persist for more than 7 days, if symptoms clear up and occur again within a few days, or if irritation develops.
Otc - Keep Out Of Reach Of Children
Keep out of reach of children.
Otc - Pregnancy Or Breast Feeding
If pregnant or breast-feeding, ask a health care professional before use.
Indications & Usage
Adults and children 12 years of age: apply generously to the affected area, massage into painful area until thoroughly absorbed into the skin, repeat as necessary, but not more than 3 to 4 times daily. Children under 12 years of age: ask a doctor.
Inactive Ingredient
Aloe Barbadensis Leaf Juice, Cetyl Alcohol, Glycerin, Methylparaben, Mineral Oil, Potassium Phosphate, Propylparaben, Stearic Acid, Triethanolamine, Water.
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