Home NDC 58593-782 Finafta
Product NDC 58593-782
11-digit product format 585930782
Labeler code 58593
Product ID 58593-782_24702e3e-55f4-4231-e063-6394a90aebbe
Type HUMAN OTC DRUG
Nonproprietary name Benzocaine
Dosage form SPRAY
Route ORAL
Labeler Efficient Laboratories Inc.
Application M022
Marketing category OTC MONOGRAPH DRUG
Marketing start 2004-09-01
Substance BENZOCAINE
Active strength 7.5 mg/100mL
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 Finafta
Brand name suffix MultiOral
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength BENZOCAINE 7.5 mg/100mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 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 1110816 Internal RxNorm lookup 1110820 Internal RxNorm lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
FDA-Initiated Inactive NDC Indexing# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 58593-782-02 FinaftaMultiOral 59 mL in 1 BOTTLE, SPRAY SPRAY 59 12 58593-782-02 FinaftaMultiOral 1 in 1 CARTON SPRAY 1 12
DailyMed Socrata Ingredients# DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 58593-782 FINAFTA MULTIORAL (BENZOCAINE) SPRAY [EFFICIENT LABORATORIES INC.] 12 Current NDC, Legacy NDC, 2 package rows 20241016_28c5a993-fb5f-4091-af15-32ccae4b9a7d.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 14 of 40 · 786 matching rows.
DailyMed RxNorm Mappings# Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Marketing start Marketing end Sample Exclude flag Status 58593-782-02 58593078202 1 BOTTLE, SPRAY in 1 CARTON (58593-782-02) / 59 mL in 1 BOTTLE, SPRAY 2004-09-01 0000-00-00 No No Current