Home NDC 60306-115 Brace Relief
Product NDC 60306-115
11-digit product format 603060115
Labeler code 60306
Product ID 60306-115_c4d6e935-9aaa-430e-ae72-51d4c84fcbf4
Type HUMAN OTC DRUG
Nonproprietary name Benzocaine
Dosage form GEL
Route ORAL
Labeler InfaLab,Inc
Application M004
Marketing category OTC MONOGRAPH DRUG
Marketing start 2005-01-03
Substance BENZOCAINE
Active strength 9 mg/mL
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 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 2019-12-08 06:16 UTC · source 2019-12-05 excluded product product 60306-115 I Inactivated by FDA excluded / ndc_excluded.zip 110d247fa046…a55b01930146…2019-12-08 06:16 UTC · source 2019-12-05 excluded package package 60306-115 60306-115-05 I Inactivated by FDA excluded / ndc_excluded.zip 110d247fa046…a55b01930146…
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 Brace Relief
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength BENZOCAINE 9 mg/mL
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 1547591 Internal RxNorm lookup 1547593 Internal RxNorm lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Product Concepts# FDA-Initiated Inactive NDC Indexing# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 60306-115-05 Brace Relief 0.3 mL in 1 TUBE GEL 0.3 12
DailyMed Socrata Ingredients# Ingredient, Type, UNII table Ingredient Type UNII DailyMed label SPL version Uploaded Benzocaine ACTIVE INGREDIENT U3RSY48JW5 BRACE RELIEF (BENZOCAINE) GEL [INFALAB,INC] 1 Benzocaine ACTIVE MOIETY U3RSY48JW5 BRACE RELIEF (BENZOCAINE) GEL [INFALAB,INC] 1 Clove Oil INACTIVE INGREDIENT 578389D6D0 BRACE RELIEF (BENZOCAINE) GEL [INFALAB,INC] 1 Glycerin INACTIVE INGREDIENT PDC6A3C0OX BRACE RELIEF (BENZOCAINE) GEL [INFALAB,INC] 1 Menthol INACTIVE INGREDIENT L7T10EIP3A BRACE RELIEF (BENZOCAINE) GEL [INFALAB,INC] 1 Methyl Salicylate INACTIVE INGREDIENT LAV5U5022Y BRACE RELIEF (BENZOCAINE) GEL [INFALAB,INC] 1 Methylparaben INACTIVE INGREDIENT A2I8C7HI9T BRACE RELIEF (BENZOCAINE) GEL [INFALAB,INC] 1 Myrrh INACTIVE INGREDIENT JC71GJ1F3L BRACE RELIEF (BENZOCAINE) GEL [INFALAB,INC] 1 Peppermint Oil INACTIVE INGREDIENT AV092KU4JH BRACE RELIEF (BENZOCAINE) GEL [INFALAB,INC] 1 Phenol INACTIVE INGREDIENT 339NCG44TV BRACE RELIEF (BENZOCAINE) GEL [INFALAB,INC] 1 Polyethylene glycol 3350 INACTIVE INGREDIENT G2M7P15E5P BRACE RELIEF (BENZOCAINE) GEL [INFALAB,INC] 1 Polyethylene glycol 400 INACTIVE INGREDIENT B697894SGQ BRACE RELIEF (BENZOCAINE) GEL [INFALAB,INC] 1 Propylparaben INACTIVE INGREDIENT Z8IX2SC1OH BRACE RELIEF (BENZOCAINE) GEL [INFALAB,INC] 1
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 60306-115 BRACE RELIEF (BENZOCAINE) GEL [INFALAB,INC] 11 Current NDC, Legacy NDC, 1 package rows 20241010_d7e57d67-4234-44a9-bbd3-72e99cd5bdb3.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 22 of 22 · 424 matching rows.
Brand, Generic, Manufacturer table Brand Generic Manufacturer SPL set ID Effective date Available safety fields Join Family Wellness Antiseptic and Pain Relief BACITRACIN ZINC, NEOMYCIN SULFATE, POLYMYXIN B SULFATE, PRAMOXINE HYDROCHLORIDE FRONT PHARMACEUTICAL PLC cb7fdcde-2bd8-4834-ba4e-4d6fd1512599 2023-10-26 Warnings Exact identifier application number: M004 GENUINE FIRST AID Antibiotic BACITRACIN ZINC, NEOMYCIN SULFATE, POLYMYXIN B SULFATE Nantong Health & Beyond Hygienic Products Inc. 23abfe12-5b50-4b49-878e-4fcdb6c341fd 2023-10-19 Warnings Exact identifier application number: M004 EVERLIT CARE Triple Antibiotic BACITRACIN ZINC, NEOMYCIN SULFATE, POLYMYXIN B SULFATE Nantong Health & Beyond Hygienic Products Inc. f4921508-c32f-426f-a2f0-16c3acbd4713 2023-10-14 Warnings Exact identifier application number: M004 Cuadriderma BACITRACIN ZINC, POLYMYXIN B SULFATE, NEOMYCIN SULFATE, AND PRAMOXINE HYDROCHLORIDE ProMex LLC 4fa99b96-ab4b-4523-82bc-343dbaf39fb6 2022-01-25 Warnings Exact identifier application number: M004
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 60306-115-05 60306011505 .3 mL in 1 TUBE (60306-115-05) 2005-01-03 0000-00-00 No No Current