Home NDC 0283-0569 HurriCaine
Product NDC 0283-0569
11-digit product format 002830569
Labeler code 0283
Product ID 0283-0569_42f260d7-63f7-4356-e063-6394a90a4676
Type HUMAN OTC DRUG
Nonproprietary name Benzocaine
Dosage form LIQUID
Route DENTAL; ORAL; PERIODONTAL
Labeler Beutlich Pharmaceuticals, LLC
Application M022
Marketing category OTC MONOGRAPH DRUG
Marketing start 1969-05-15
Substance BENZOCAINE
Active strength 200 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 Observed NDC auxiliary status history# This history shows the information present in each captured FDA auxiliary file. It is not a continuous regulatory timeline, and a missing record does not establish a status.
Historic NDC status page 1 of 1 · 2 matching rows.
View current auxiliary records. · View the auxiliary file history.
Captured / source date, Dataset, Scope table Captured / source date Dataset Scope Product NDC Package NDC Code Status Reporting period Archive Snapshot Source SHA-256 2025-12-14 17:58 UTC · source 2025-12-05 excluded package package 0283-0569 0283-0569-72 D Discontinued by firm excluded / ndc_excluded.zip d630ba8d3edf…732f749b63fb…2025-12-14 17:58 UTC · source 2025-12-05 excluded package package 0283-0569 0283-0569-02 D Discontinued by firm excluded / ndc_excluded.zip d630ba8d3edf…732f749b63fb…
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 HurriCaine
Brand name suffix Topical Anesthetic Liquid
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength BENZOCAINE 200 mg/g
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 308657 Internal RxNorm lookup 808062 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 0283-0569-02 HurriCaineTopical Anesthetic Liquid 2 g in 1 APPLICATOR LIQUID 2 51 0283-0569-17 HurriCaineTopical Anesthetic Liquid 1 g in 1 PACKET LIQUID 1 51 0283-0569-31 HurriCaineTopical Anesthetic Liquid 29.6 g in 1 BOTTLE, PLASTIC LIQUID 29.6 51 0283-0569-72 HurriCaineTopical Anesthetic Liquid 72 g in 1 APPLICATOR LIQUID 72 51
DailyMed Socrata Ingredients# DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 0283-0569 HURRICAINE TOPICAL ANESTHETIC LIQUID (BENZOCAINE) LIQUID [BEUTLICH PHARMACEUTICALS, LLC] 50 Current NDC, Legacy NDC, 4 package rows 20240702_fee9969d-ad1a-4f44-9741-a0a44c9e1128.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 9 of 40 · 786 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 0283-0569-02 00283056902 2 g in 1 APPLICATOR (0283-0569-02) 2 g 1969-05-15 0000-00-00 No No Current 0283-0569-17 00283056917 1 g in 1 PACKET (0283-0569-17) 1 g 2020-01-28 0000-00-00 No No Current 0283-0569-31 00283056931 29.6 g in 1 BOTTLE, PLASTIC (0283-0569-31) 29.6 g 1969-05-15 0000-00-00 No No Current 0283-0569-72 00283056972 72 g in 1 APPLICATOR (0283-0569-72) 72 g 1969-05-15 0000-00-00 No No Current