Dermoplast Pain Relieving 200 mg/g
BENZOCAINE and LEVOMENTHOL · SPRAY · Advantice Health, LLC
Dermoplast Pain Relieving is a spray containing benzocaine and levomenthol at 200 mg/g, taken topical. Manufactured by Advantice Health, LLC.
Key Facts
- Brand Name
- Dermoplast Pain Relieving
- Generic Name
- BENZOCAINE and LEVOMENTHOL
- NDC Code (Product)
16864-680- Manufacturer
- Advantice Health, LLC
- Strength
- 200 mg/g
- Dosage Form
- SPRAY
- Route
- TOPICAL
- Marketing Status
- Application #
- M017
- Drug Class
- Standardized Chemical Allergen [EPC]
- Marketing Start
- 01/01/2014
Recall History
No Recall HistoryFrequently Asked Questions
What is Dermoplast Pain Relieving used for?
Dermoplast Pain Relieving contains BENZOCAINE and LEVOMENTHOL. It is a spray taken topical. Consult your doctor for specific uses.
Is Dermoplast Pain Relieving a controlled substance?
Dermoplast Pain Relieving is not classified as a controlled substance by the DEA.
What is the generic name for Dermoplast Pain Relieving?
The generic name for Dermoplast Pain Relieving is BENZOCAINE and LEVOMENTHOL. There are no other listed brand versions of BENZOCAINE and LEVOMENTHOL.
What is the NDC code for Dermoplast Pain Relieving 200 mg/g?
The NDC (National Drug Code) for Dermoplast Pain Relieving 200 mg/g is 16864-680, listed by Advantice Health, LLC.
Not medical advice. Always consult your doctor or pharmacist before making any medication decisions.
Data from openFDA · Public domain (CC0 1.0)