Home NDC 16864-690 Dermoplast Pain relieving
Product NDC 16864-690
11-digit product format 168640690
Labeler code 16864
Product ID 16864-690_0d12185e-8d41-7d76-e063-6294a90a2cf4
Type HUMAN OTC DRUG
Nonproprietary name BENZOCAINE, MENTHOL
Dosage form SPRAY
Route TOPICAL
Labeler Advantice Health
Application M017
Marketing category OTC MONOGRAPH DRUG
Marketing start 2022-03-18
Substance BENZOCAINE; MENTHOL
Active strength 200; 5 mg/g; mg/g
Pharmacologic classes Allergens [CS], Cell-mediated Immunity [PE], Increased Histamine Release [PE], Standardized Chemical Allergen [EPC]
NDC exclude flag No
Listing certified through 2026-12-31
Current FDA listing Yes Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.
Additional Listing Data#
Finished product Yes
Brand name base Dermoplast Pain relieving
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength BENZOCAINE 200 mg/g MENTHOL 5 mg/g
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 2 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination U3RSY48JW5 Internal UNII lookup L7T10EIP3A Internal UNII lookup
Harmonized RxCUI identifiers# RxCUI identifiers page 1 of 1 · 2 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 199864 Internal RxNorm lookup 763484 Internal RxNorm lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 16864-690-01 Dermoplast Pain relieving 78 g in 1 CAN SPRAY 78 2
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 16864-690 DERMOPLAST PAIN RELIEVING (BENZOCAINE, MENTHOL) SPRAY [ADVANTICE HEALTH] 2 Current NDC, Legacy NDC, 1 package rows 20231222_dad00c95-4e11-3eec-e053-2a95a90a7a18.zip
openFDA label cross-check# OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
Matched openFDA labels page 48 of 153 · 3,057 matching rows.
DailyMed RxNorm Mappings# Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 16864-690-01 16864069001 78 g in 1 CAN (16864-690-01) 78 g 2022-03-18 0000-00-00 No No Current