Home NDC 69993-100 Maximum Strength Blue Emu Pain Relief
Product NDC 69993-100
11-digit product format 699930100
Labeler code 69993
Product ID 69993-100_a2191961-c9d8-43b6-b230-3f38166f74a2
Type HUMAN OTC DRUG
Nonproprietary name Trolamine Salicylate
Dosage form SPRAY
Route TOPICAL
Labeler Kingsway Pharmaceuticals dba NFI, LLC
Application M017
Marketing category OTC MONOGRAPH DRUG
Marketing start 2012-06-04
Substance TROLAMINE SALICYLATE
Active strength 10 g/100mL
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 · 6 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 2025-02-02 03:52 UTC · source 2025-01-31 excluded product product 302b2466d912…e7b80fea0513…2025-02-02 03:52 UTC · source 2025-01-31 excluded package package 69993-100-04 302b2466d912…e7b80fea0513…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 69993-100-04 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 69993-100-04 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 Maximum Strength Blue Emu Pain Relief
Brand name suffix Blu Emu
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength TROLAMINE SALICYLATE 10 g/100mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination H8O4040BHD Internal UNII lookup
Harmonized RxCUI identifiers# RxCUI identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 1048119 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 69993-100-04 Maximum Strength Blue Emu Pain ReliefBlu Emu 118 mL in 1 CAN SPRAY 118 8
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 69993-100 MAXIMUM STRENGTH BLUE EMU PAIN RELIEF BLU EMU (TROLAMINE SALICYLATE) SPRAY [KINGSWAY PHARMACEUTICALS DBA NFI, LLC] 8 Current NDC, Legacy NDC, 1 package rows 20250205_5e02b820-e53a-42cb-abdb-2925617c29ca.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 48 of 153 · 3,057 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 69993-100-04 69993010004 118 mL in 1 CAN (69993-100-04) 118 ml 2012-06-04 0000-00-00 No No Current