Ultra-Strength Pain Relief Analgesic 110 mg/g
CAMPHOR (SYNTHETIC) and MENTHOL, UNSPECIFIED FORM · OINTMENT · TARGET CORPORATION
Ultra-Strength Pain Relief Analgesic is a ointment containing camphor (synthetic) and menthol, unspecified form at 110 mg/g, taken topical. Manufactured by TARGET CORPORATION.
Key Facts
- Brand Name
- Ultra-Strength Pain Relief Analgesic
- Generic Name
- CAMPHOR (SYNTHETIC) and MENTHOL, UNSPECIFIED FORM
- NDC Code (Product)
82442-311- Manufacturer
- TARGET CORPORATION
- Strength
- 110 mg/g
- Dosage Form
- OINTMENT
- Route
- TOPICAL
- Marketing Status
- Application #
- M017
- Marketing Start
- 10/14/2024
Recall History
No Recall HistoryFrequently Asked Questions
What is Ultra-Strength Pain Relief Analgesic used for?
Ultra-Strength Pain Relief Analgesic contains CAMPHOR (SYNTHETIC) and MENTHOL, UNSPECIFIED FORM. It is a ointment taken topical. Consult your doctor for specific uses.
Is Ultra-Strength Pain Relief Analgesic a controlled substance?
Ultra-Strength Pain Relief Analgesic is not classified as a controlled substance by the DEA.
What is the generic name for Ultra-Strength Pain Relief Analgesic?
The generic name for Ultra-Strength Pain Relief Analgesic is CAMPHOR (SYNTHETIC) and MENTHOL, UNSPECIFIED FORM. There are 4 other brand versions of CAMPHOR (SYNTHETIC) and MENTHOL, UNSPECIFIED FORM.
What is the NDC code for Ultra-Strength Pain Relief Analgesic 110 mg/g?
The NDC (National Drug Code) for Ultra-Strength Pain Relief Analgesic 110 mg/g is 82442-311, listed by TARGET CORPORATION.