Home NDC 82570-010-01 Dekangling
Product NDC 82570-010
Requested package NDC 82570-010-01
11-digit product format 825700010
Labeler code 82570
Product ID 82570-010_d884dd7b-fc24-d6d7-e053-2a95a90af9f1
Type HUMAN OTC DRUG
Nonproprietary name Phellinus and Brazil Mushroom Antrodia cinnamomea Extract Powder
Dosage form POWDER
Route TOPICAL
Labeler Shenzhen Deyintang Biotechnology Co., Ltd.
Marketing category UNAPPROVED DRUG OTHER
Marketing start 2022-02-21
Marketing end 0000-00-00
Substance COLLAGEN, SOLUBLE, FISH SKIN; CORDYCEPS MILITARIS FRUITING BODY; CULTIVATED MUSHROOM; MORINGA OLEIFERA LEAF; POMIFERIN; TAIWANOFUNGUS CAMPHORATUS MYCELIUM
Active strength 20 g/100g; g/100g; g/100g; g/100g; g/100g; g/100g
Pharmacologic classes Allergens [CS], Cell-mediated Immunity [PE], Dietary Proteins [CS], Fungal Proteins [CS], Increased Histamine Release [PE], Non-Standardized Food Allergenic Extract [EPC]
NDC exclude flag No
Listing certified through 2023-12-31
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 · 15 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…
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 82570-010-01 Dekangling 3 g in 1 POUCH POWDER 3 1
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 82570-010 DEKANGLING (PHELLINUS AND BRAZIL MUSHROOM ANTRODIA CINNAMOMEA EXTRACT POWDER) POWDER [SHENZHEN DEYINTANG BIOTECHNOLOGY CO., LTD.] 1 Legacy NDC, 1 package rows 20220222_d884dd7b-fc23-d6d7-e053-2a95a90af9f1.zip
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 82570-010-01 82570001001 3 g in 1 POUCH (82570-010-01) 3 g 2022-02-21 0000-00-00 No No Current