Home NDC 71564-009 OKeeffes Working Hands Pain Relief
Product NDC 71564-009
11-digit product format 715640009
Labeler code 71564
Product ID 71564-009_2cca0907-5d70-e478-e063-6294a90ad19d
Type HUMAN OTC DRUG
Nonproprietary name allantoin, lidocaine hydrochloride
Dosage form CREAM
Route TOPICAL
Labeler The Gorilla Glue Company/O'Keeffe's Company
Application M017
Marketing category OTC MONOGRAPH DRUG
Marketing start 2023-10-07
Substance ALLANTOIN; LIDOCAINE HYDROCHLORIDE
Active strength .5; 4 g/100g; g/100g
Pharmacologic classes Amide Local Anesthetic [EPC], Amides [CS], Antiarrhythmic [EPC], Local Anesthesia [PE]
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 · 4 matching rows.
View current auxiliary records. · View the auxiliary file history.
Captured / source date, Dataset, Scope table Captured / source date Dataset Scope Package NDC Snapshot Source SHA-256 2025-01-20 13:05 UTC · source 2025-01-20 excluded product product ed331223b511…672a5bd82f5f…2025-01-20 13:05 UTC · source 2025-01-20 excluded package package 71564-009-03 ed331223b511…672a5bd82f5f…2025-01-11 03:41 UTC · source 2025-01-10 excluded product product 0efc9e666f02…f202fb6c5f17…2025-01-11 03:41 UTC · source 2025-01-10 excluded package package 71564-009-03 0efc9e666f02…f202fb6c5f17…
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 OKeeffes Working Hands Pain Relief
Brand name suffix Skin Protectant
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength ALLANTOIN .5 g/100g LIDOCAINE HYDROCHLORIDE 4 g/100g
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 2 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 344S277G0Z Internal UNII lookup V13007Z41A Internal UNII lookup
Harmonized RxCUI identifiers# RxCUI identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 2594492 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 71564-009-03 OKeeffes Working Hands Pain ReliefSkin Protectant 85 g in 1 TUBE CREAM 85 3 71564-009-03 OKeeffes Working Hands Pain ReliefSkin Protectant 1 in 1 CARTON CREAM 1 3
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 71564-009 OKEEFFES WORKING HANDS PAIN RELIEF SKIN PROTECTANT (ALLANTOIN, LIDOCAINE HYDROCHLORIDE) CREAM [THE GORILLA GLUE COMPANY/O'KEEFFE'S COMPANY] 3 Current NDC, 2 package rows 20250130_0685da25-c9fa-e1cd-e063-6394a90ae1b3.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 18 of 152 · 3,029 matching rows.
DailyMed RxNorm Mappings# Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Sample Exclude flag Status 71564-009-03 71564000903 1 TUBE in 1 CARTON (71564-009-03) / 85 g in 1 TUBE 1 tube 2023-10-07 No No Current