Home NDC 11527-062 Sheffield Pain Relief
Product NDC 11527-062
11-digit product format 115270062
Labeler code 11527
Product ID 11527-062_2782a87e-5b11-4ee5-8649-3f31a52d4bda
Type HUMAN OTC DRUG
Nonproprietary name BENZOCAINE
Dosage form GEL
Route ORAL
Labeler Sheffield Pharmaceuticals LLC
Application M022
Marketing category OTC MONOGRAPH DRUG
Marketing start 2006-01-30
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 · 6 matching rows.
View current auxiliary records. · View the auxiliary file history.
Captured / source date, Snapshot, Source SHA-256 table Captured / source date Snapshot Source SHA-256 2025-12-14 17:58 UTC · source 2025-12-05 d630ba8d3edf…732f749b63fb…2025-08-27 00:01 UTC · source 2025-08-26 f5e01cc5f278…a2eaf40c39c3…2025-04-01 02:39 UTC · source 2025-03-31 2ef7874e63bc…57b86245f4fa…2025-03-28 20:22 UTC · source 2025-03-28 a1b67e2a42f9…c4cf2c586c0d…2025-03-22 03:12 UTC · source 2025-03-21 cfe11265f3b6…090c488252e2…2025-03-10 12:48 UTC · source 2025-03-10 cdf11ea48f46…ba0047e9e063…
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 Sheffield Pain Relief
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 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 238910 Internal RxNorm lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Product Concepts# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 11527-062-47 Sheffield Pain Relief 1 in 1 CARTON GEL 1 6 11527-062-47 Sheffield Pain Relief 9.35 g in 1 TUBE GEL 9.35 6 11527-062-55 Sheffield Pain Relief 1 in 1 CARTON GEL 1 6 11527-062-55 Sheffield Pain Relief 9.35 g in 1 TUBE GEL 9.35 6
DailyMed Socrata Ingredients# DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 11527-062 SHEFFIELD PAIN RELIEF (BENZOCAINE) GEL [SHEFFIELD PHARMACEUTICALS LLC] 6 Current NDC, Legacy NDC, 4 package rows 20250221_e21abfdd-373d-42af-9535-fe1571382a65.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 27 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 11527-062-47 11527006247 1 TUBE in 1 CARTON (11527-062-47) / 9.35 g in 1 TUBE 1 tube 2006-01-30 No No Current 11527-062-55 11527006255 1 TUBE in 1 CARTON (11527-062-55) > 9.35 g in 1 TUBE 1 tube 2006-01-30 0000-00-00 No No Current