Home NDC 66506-183 CheeZheng Pain Relieveing Plaster
Product NDC 66506-183
11-digit product format 665060183
Labeler code 66506
Product ID 66506-183_2ddf21aa-3ca3-4d14-e063-6394a90a52fa
Type HUMAN OTC DRUG
Nonproprietary name camphor
Dosage form PLASTER
Route TOPICAL
Labeler Tibet Cheezheng Tibetan Medicine Co. Ltd.
Application M017
Marketing category OTC MONOGRAPH DRUG
Marketing start 2019-11-29
Substance CAMPHOR (NATURAL)
Active strength 1 g/100g
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, 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 66506-183-01 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 66506-183-01 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 66506-183-01 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 CheeZheng Pain Relieveing Plaster
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength CAMPHOR (NATURAL) 1 g/100g
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination N20HL7Q941 Internal UNII lookup
Harmonized RxCUI identifiers# RxCUI identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 1725038 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 66506-183-01 CheeZheng Pain Relieveing Plaster 5 in 1 PACKAGE PLASTER 5 6 66506-183-02 CheeZheng Pain Relieveing Plaster 1.2 g in 1 PACKAGE PLASTER 1.2 6
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 66506-183 CHEEZHENG PAIN RELIEVEING PLASTER (CAMPHOR) PLASTER [TIBET CHEEZHENG TIBETAN MEDICINE CO. LTD.] 6 Current NDC, Legacy NDC, 2 package rows 20250213_abcebdf1-9037-4094-93e1-ce8f20b18ea7.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 50 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 Marketing end Sample Exclude flag Status 66506-183-01 66506018301 5 PACKAGE in 1 PACKAGE (66506-183-01) / 1.2 g in 1 PACKAGE (66506-183-02) 5 package 2019-11-29 0000-00-00 No No Current 66506-183-02 66506018302 1.2 g in 1 PACKAGE 1.2 g Historical