Home NDC 44911-0473-1 Hypothalmupar
Product NDC 44911-0473
Requested package NDC 44911-0473-1
11-digit product format 449110473
Labeler code 44911
Product ID 44911-0473_e646941c-406d-4e3e-af16-bcd09d44ea78
Type HUMAN OTC DRUG
Nonproprietary name Aralia Quinquefolia, Ginkgo Biloba, Hydrocotyle Asiatica, Cerebrum Suis, Hypophysis Suis, Hypothalamus Suis, Phosphorus, Silicea
Dosage form LIQUID
Route ORAL
Labeler Energique, Inc.
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 2018-09-24
Substance AMERICAN GINSENG; GINKGO; CENTELLA ASIATICA WHOLE; SUS SCROFA CEREBRUM; SUS SCROFA PITUITARY GLAND; SUS SCROFA HYPOTHALAMUS; PHOSPHORUS; SILICON DIOXIDE
Active strength 3; 3; 3; 8; 8; 12; 12; 12 [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 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 · 5 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 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.
Additional Listing Data#
Finished product Yes
Brand name base Hypothalmupar
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength AMERICAN GINSENG 3 [hp_X]/mL GINKGO 3 [hp_X]/mL CENTELLA ASIATICA WHOLE 3 [hp_X]/mL SUS SCROFA CEREBRUM 8 [hp_X]/mL SUS SCROFA PITUITARY GLAND 8 [hp_X]/mL SUS SCROFA HYPOTHALAMUS 12 [hp_X]/mL PHOSPHORUS 12 [hp_X]/mL SILICON DIOXIDE 12 [hp_X]/mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 8 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 44911-0473-1 Hypothalmupar 30 mL in 1 BOTTLE, DROPPER LIQUID 30 5
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 44911-0473 HYPOTHALMUPAR (ARALIA QUINQUEFOLIA, GINKGO BILOBA, HYDROCOTYLE ASIATICA, CEREBRUM SUIS, HYPOPHYSIS SUIS, HYPOTHALAMUS SUIS, PHOSPHORUS, SILICEA) LIQUID [ENERGIQUE, INC.] 5 Current NDC, Legacy NDC, 1 package rows 20241030_8b01e718-83b7-4f93-8fea-d0e37c756185.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.
Brand, Generic, Manufacturer table Brand Generic Manufacturer SPL set ID Effective date Available safety fields Join Hypothalmupar ARALIA QUINQUEFOLIA, GINKGO BILOBA, HYDROCOTYLE ASIATICA, CEREBRUM SUIS, HYPOPHYSIS SUIS, HYPOTHALAMUS SUIS, PHOSPHORUS, SILICEA Energique, Inc. 8b01e718-83b7-4f93-8fea-d0e37c756185 2024-10-28 Warnings Exact identifier ndc (package): 44911-0473-1 ndc (product): 44911-0473 ndc11 (package): 44911047301
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 44911-0473-1 44911047301 30 mL in 1 BOTTLE, DROPPER (44911-0473-1) 30 ml 2018-09-24 0000-00-00 No No Current