Home NDC 73442-0009 SSANGGI TANG
Product NDC 73442-0009
11-digit product format 734420009
Labeler code 73442
Product ID 73442-0009_2dfc94d6-12cc-758f-e063-6294a90a14a4
Type HUMAN OTC DRUG
Nonproprietary name ssanghwa extract
Dosage form LIQUID
Route ORAL
Labeler I World Pharmaceutical Co., Ltd.
Marketing category UNAPPROVED DRUG OTHER
Marketing start 2019-10-08
Substance ASTRAGALUS GUMMIFER ROOT; LIGUSTICUM SINENSE SUBSP. CHUANXIONG ROOT; PAEONIA LACTIFLORA ROOT; REHMANNIA GLUTINOSA ROOT
Active strength .4845; .627; .9785; .6745 g/100mL; g/100mL; g/100mL; g/100mL
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 73442-0009-1 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 73442-0009-1 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 73442-0009-1 0efc9e666f02…f202fb6c5f17…
Additional Listing Data#
Finished product Yes
Brand name base SSANGGI TANG
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength PAEONIA LACTIFLORA ROOT .4845 g/100mL REHMANNIA GLUTINOSA ROOT .627 g/100mL LIGUSTICUM SINENSE SUBSP. CHUANXIONG ROOT .9785 g/100mL ASTRAGALUS GUMMIFER ROOT .6745 g/100mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 4 matching rows.
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 73442-0009-1 SSANGGI TANG 80 mL in 1 POUCH LIQUID 80 2
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 73442-0009 SSANGGI TANG (SSANGHWA EXTRACT) LIQUID [I WORLD PHARMACEUTICAL CO., LTD.] 2 Current NDC, Legacy NDC, 1 package rows 20250215_96e441ab-d39f-2259-e053-2a95a90a9abd.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 1 of 1 · 1 matching rows.
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 73442-0009-1 73442000901 80 mL in 1 POUCH (73442-0009-1) 80 ml 2019-10-08 0000-00-00 No No Current