Home NDC 77547-002-01 Yiyongkesoutie
Product NDC 77547-002
Requested package NDC 77547-002-01
11-digit product format 775470002
Labeler code 77547
Product ID 77547-002_a8773606-805c-af4f-e053-2a95a90a2b32
Type HUMAN OTC DRUG
Nonproprietary name camphor
Dosage form PLASTER
Route TOPICAL
Labeler Beijing Shenzhou Pharmaceutical Technology Co., Ltd
Application part348
Marketing category OTC MONOGRAPH NOT FINAL
Marketing start 2020-06-19
Marketing end 0000-00-00
Substance CAMPHOR (NATURAL)
Active strength 1 g/100g
NDC exclude flag No
Listing certified through 2021-12-31
Current FDA listing Historical FDA.report record 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 · 18 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…2025-02-02 03:52 UTC · source 2025-01-31 302b2466d912…e7b80fea0513…2025-01-20 13:05 UTC · source 2025-01-20 ed331223b511…672a5bd82f5f…2025-01-11 03:41 UTC · source 2025-01-10 0efc9e666f02…f202fb6c5f17…2024-11-09 02:27 UTC · source 2024-11-08 ad56d346431e…cc804d4bbf1e…2024-10-04 04:10 UTC · source 2024-10-03 367a005e9d99…383a685ebd0f…2024-07-10 04:00 UTC · source 2024-07-09 557ba5c1ecfa…9c80585c8c6e…2024-05-28 21:12 UTC · source 2024-05-28 8af77b9d5b6f…d9bbb34c5368…2024-05-15 03:39 UTC · source 2024-05-14 834df4deac94…adcc014656a3…2024-03-11 06:39 UTC · source 2024-03-08 1332a3947898…d4bfe170f9cd…2022-08-30 03:57 UTC · source 2022-08-29 fb8cb913e6d1…eb8c232b6be0…2022-04-09 23:13 UTC · source 2022-04-08 86f5da6cb304…a595104c45d7…2022-04-04 05:40 UTC · source 2022-04-01 bd6a592717d7…303034d00443…
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.
FDA-Initiated Inactive NDC Indexing# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 77547-002-01 Yiyongkesoutie 2 in 1 PACKAGE PLASTER 2 1 77547-002-01 Yiyongkesoutie 24 in 1 BOX PLASTER 24 1 77547-002-02 Yiyongkesoutie 1 g in 1 PACKAGE PLASTER 1 1
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 77547-002 YIYONGKESOUTIE (CAMPHOR) PLASTER [BEIJING SHENZHOU PHARMACEUTICAL TECHNOLOGY CO., LTD] 1 Legacy NDC, 3 package rows 20200623_5b64dc2b-ac6f-4f0f-ab8f-5db98b0c2810.zip
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 77547-002-01 77547000201 24 PACKAGE in 1 BOX (77547-002-01) > 2 PACKAGE in 1 PACKAGE > 1 g in 1 PACKAGE (77547-002-02) 24 package 2020-06-19 0000-00-00 No No Current