FDA Label for Pharmacys Prescription Analgesic Gel
View Indications, Usage & Precautions
Pharmacys Prescription Analgesic Gel Product Label
The following document was submitted to the FDA by the labeler of this product American Consumer Products Corp. 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.
Active Ingredient
Active Ingredient: Menthol 1%
Purpose
Purpose: Pain relieving gel
Warnings
Warnings: For external use only
Stop Use
Stop use and ask doctor if
- condition worsens, or if symptoms persist for more than 7 days or clear up and occur again within a few days.
Keep Out Of Reach Of Children
Keep our of reach of children. If swallowed get medical help or contact a Poison Control Center immediately.
Inactive Ingredients
Inactive Ingredients
carbomer, isopropyl alcohol, nonyl phenyl polyoxyethylene ether, camphor, kathon CG, FD&C blue no. 1, triethanolamine, water
Indications & Usage Section
Uses: For the temporary relief of minor aches and pains of muscles and joints associated with - simple backache - arthritis - strains - bruses - sprains
When using this product
- avoid contact with eyes
- do not bandage tightly
- do not apply to wounds or damaged skin
- do not use with heating pads or other heating devices
Dosage & Administration
Directions
- adults and childrent 2 years of age and older: apply to affected area not more than 3 to 4 times daily
- children under 2 years of age: do not use, consult a doctor
Pharmacy's Prescription 8 Oz Ice Cold Analgesic Gel
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