FDA Label for Neilmed Hot And Cold Pain Relief
View Indications, Usage & Precautions
Neilmed Hot And Cold Pain Relief Product Label
The following document was submitted to the FDA by the labeler of this product Neilmed Pharmaceuticals Inc.. 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.
Directions
Directions: Shake well – adults and children 12 years of age and older: spray product on affected area, not more than 3 to 4 times daily. – children under 12 years of age: consult a doctor.
Warnings
For external use only.
Flammable: Do not use while smoking or near heat or flames. Avoid long term storage above 104°F. Do not puncture or incinerate. Contents under pressure. Do not store at temperatures above 120°F.
When using this product avoid contact with eyes and mucous membranes. Do not apply to wounds or damaged skin. Do not bandage tightly. Use only as directed.
Stop use and ask doctor if condition worsens or symptoms persist for more than 7 days or clear up and occur again within a few days. Do not use for longer than 1 week.
Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center immediately.
If pregnant or breast-feeding, ask a health professional before use.
Inactive Ingredients
Glycerin, Propylene Glycol, SD Alcohol 40 (58%), USP grade Purified Water.
Uses
Temporarily alleviates minor aches and pains of muscles and joints associated with Arthritis, Simple Backache, Strains, Bruises, or Sprains
Warnings: Keep Out Of Reach Of Children.
If swallowed, get medical help or contact a Poison Control Center immediately.
Drug Facts:
Topical Analgesic
Active Ingredient
Menthol 16.0%
Package Label - Neilmed Hot & Cold Pain Relief
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