Home NDC 44911-0280-1 Renapar
Product NDC 44911-0280
Requested package NDC 44911-0280-1
11-digit product format 449110280
Labeler code 44911
Product ID 44911-0280_b1e23b09-f362-494c-8bf4-700edfe80d43
Type HUMAN OTC DRUG
Nonproprietary name Pareira Brava, Petroselinum Sativum, Sarsaparilla (Smilax Regelii), Kidney (Suis), Bryonia (Alba), Mercurius Corrosivus, Rubia Tinctorum, Solidago Virgaurea, Triticum Repens
Dosage form LIQUID
Route ORAL
Labeler Energique, Inc.
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 2015-10-23
Marketing end 2024-04-29
Substance CHONDRODENDRON TOMENTOSUM ROOT; PETROSELINUM CRISPUM; SMILAX ORNATA ROOT; PORK KIDNEY; BRYONIA ALBA ROOT; MERCURIC CHLORIDE; RUBIA TINCTORUM ROOT; SOLIDAGO VIRGAUREA FLOWERING TOP; ELYMUS REPENS ROOT
Active strength 3 [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL
NDC exclude flag No
Listing certified through 0000-00-00
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 · 12 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…
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.
FDA-Initiated Inactive NDC Indexing# Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 44911-0280-1 44911028001 30 mL in 1 BOTTLE, DROPPER (44911-0280-1) 30 ml 2015-10-23 2024-04-29 No No Current