Dermoplast Pain relieving 200 mg/g
BENZOCAINE, MENTHOL · SPRAY · Advantice Health
Dermoplast Pain relieving is a spray containing benzocaine, menthol at 200 mg/g, taken topical. Manufactured by Advantice Health.
Key Facts
- Brand Name
- Dermoplast Pain relieving
- Generic Name
- BENZOCAINE, MENTHOL
- NDC Code (Product)
16864-690- Manufacturer
- Advantice Health
- Strength
- 200 mg/g
- Dosage Form
- SPRAY
- Route
- TOPICAL
- Marketing Status
- Application #
- M017
- Drug Class
- Standardized Chemical Allergen [EPC]
- Marketing Start
- 03/18/2022
Recall History
No Recall HistoryFrequently Asked Questions
What is Dermoplast Pain relieving used for?
Dermoplast Pain relieving contains BENZOCAINE, MENTHOL. 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, MENTHOL. There are 9 other brand versions of BENZOCAINE, MENTHOL.
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 16864-690, listed by Advantice Health.
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Not medical advice. Always consult your doctor or pharmacist before making any medication decisions.
Data from openFDA · Public domain (CC0 1.0)