Active Ingredient
Active Ingredient: Menthol 1%
The following Structured Product Label (SPL) was submitted to the FDA by American Consumer Products Corp for the product Pharmacys Prescription Analgesic Gel (NDC 72197-001). This document serves as the official prescribing information, containing essential scientific data and clinical materials required for healthcare providers and patients.
This specific version of the label includes detailed information regarding active ingredient, purpose, warnings, stop use, keep out of reach of children, inactive ingredients, indications & usage section, dosage & administration, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Active Ingredient: Menthol 1%
Purpose: Pain relieving gel
Warnings: For external use only
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 our of reach of children. If swallowed get medical help or contact a Poison Control Center immediately.
Inactive Ingredients
carbomer, isopropyl alcohol, nonyl phenyl polyoxyethylene ether, camphor, kathon CG, FD&C blue no. 1, triethanolamine, water
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
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
* Please review the disclaimer below.