NDC 16864-681

Dermoplast Sunburn and Burn Relief

Benzocaine And Levomenthol

Dermoplast Sunburn and Burn Relief is a Topical Spray in the Human Otc Drug category. It is labeled and distributed by Advantice Health, Llc. The primary component is Benzocaine; Levomenthol.

• Product ID: 16864-681_b30118b0-b328-4782-8f68-8f99ab19fcd7
• NDC: 16864-681
• Product Type: Human Otc Drug
• Proprietary Name: Dermoplast Sunburn and Burn Relief
• Generic Name: Benzocaine And Levomenthol
• Dosage Form: Spray
• Route of Administration: TOPICAL
• Marketing Start Date: 2021-05-15
• Marketing Category: OTC MONOGRAPH NOT FINAL /
• Application Number: part348
• Labeler Name: Advantice Health, LLC
• Substance Name: BENZOCAINE; LEVOMENTHOL
• Active Ingredient Strength: 200 mg/g; mg/g
• NDC Exclude Flag: N
• Listing Certified Through: 2022-12-31

Packaging

NDC 16864-681-01

78 g in 1 CAN (16864-681-01)

• Marketing Start Date: 2021-05-15
• NDC Exclude Flag: N
• Sample Package?: N

Drug Details

NDC Crossover Matching brand name "Dermoplast Sunburn and Burn Relief" or generic name "Benzocaine And Levomenthol"

NDC	Brand Name	Generic Name
16864-681	Dermoplast Sunburn and Burn Relief	benzocaine and levomenthol
16864-682	Dermoplast Insect Itch and Sting Relief	BENZOCAINE and LEVOMENTHOL
16864-680	Dermoplast Pain Relieving	BENZOCAINE and LEVOMENTHOL