Home NDC 16864-670 Dermoplast First Aid
Product NDC 16864-670
11-digit product format 168640670
Labeler code 16864
Product ID 16864-670_4849d774-4d2d-2d24-e063-6294a90ab234
Type HUMAN OTC DRUG
Nonproprietary name BENZETHONIUM CHLORIDE and BENZOCAINE
Dosage form SPRAY
Route TOPICAL
Labeler Advantice Health, LLC
Application M003
Marketing category OTC MONOGRAPH DRUG
Marketing start 2010-01-01
Substance BENZETHONIUM CHLORIDE; BENZOCAINE
Active strength 2; 200 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 2027-12-31
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 First Aid
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength BENZETHONIUM CHLORIDE 2 mg/g BENZOCAINE 200 mg/g
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 2 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination PH41D05744 Internal UNII lookup U3RSY48JW5 Internal UNII lookup
Harmonized RxCUI identifiers# RxCUI identifiers page 1 of 1 · 2 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 1049108 Internal RxNorm lookup 1101914 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 16864-670-01 Dermoplast First Aid 78 g in 1 CAN SPRAY 78 6
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 16864-670 DERMOPLAST FIRST AID (BENZETHONIUM CHLORIDE AND BENZOCAINE) SPRAY [ADVANTICE HEALTH, LLC] 5 Current NDC, Legacy NDC, 1 package rows 20241215_ec93011d-7069-4021-8dd2-3d51eb6026e1.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 99 of 114 · 2,270 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 16864-670-01 16864067001 78 g in 1 CAN (16864-670-01) 78 g 2010-01-01 0000-00-00 No No Current