Home NDC 44911-0595-1 Upper Resp HP
Product NDC 44911-0595
Requested package NDC 44911-0595-1
11-digit product format 449110595
Labeler code 44911
Product ID 44911-0595_95dcbcc9-a898-4bd2-92bc-a8d488664c15
Type HUMAN OTC DRUG
Nonproprietary name Carbo Vegetabilis, Cuprum Metallicum, Drosera (Rotundifolia), Hepar Sulphuris Calcareum, Ipecacuanha, Lachesis Mutus, Lobelia Inflata, Phosphorus, Pulsatilla (Pratensis), Rumex Crispus, Spongia Tosta
Dosage form LIQUID
Route ORAL
Labeler Energique, Inc.
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 2021-01-04
Substance ACTIVATED CHARCOAL; CALCIUM SULFIDE; COPPER; DROSERA ROTUNDIFOLIA WHOLE; IPECAC; LACHESIS MUTA VENOM; LOBELIA INFLATA WHOLE; PHOSPHORUS; PULSATILLA PRATENSIS WHOLE; RUMEX CRISPUS ROOT; SPONGIA OFFICINALIS SKELETON, ROASTED
Active strength 30; 30; 30; 30; 30; 30; 30; 30; 30; 30; 30 [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; [hp_X]/mL; [hp_X]/mL
Pharmacologic classes Copper [CS], Copper-containing Intrauterine Device [EPC], Decreased Embryonic Implantation [PE], Decreased Sperm Motility [PE], Inhibit Ovum Fertilization [PE]
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…
Additional Listing Data#
Finished product Yes
Brand name base Upper Resp HP
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength ACTIVATED CHARCOAL 30 [hp_X]/mL COPPER 30 [hp_X]/mL DROSERA ROTUNDIFOLIA WHOLE 30 [hp_X]/mL CALCIUM SULFIDE 30 [hp_X]/mL IPECAC 30 [hp_X]/mL LACHESIS MUTA VENOM 30 [hp_X]/mL LOBELIA INFLATA WHOLE 30 [hp_X]/mL PHOSPHORUS 30 [hp_X]/mL PULSATILLA PRATENSIS WHOLE 30 [hp_X]/mL RUMEX CRISPUS ROOT 30 [hp_X]/mL SPONGIA OFFICINALIS SKELETON, ROASTED 30 [hp_X]/mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 11 matching rows.
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Product Concepts# FDA-Initiated Inactive NDC Indexing# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 44911-0595-1 Upper Resp HP 30 mL in 1 BOTTLE, DROPPER LIQUID 30 2
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 44911-0595 UPPER RESP HP (CARBO VEGETABILIS, CUPRUM METALLICUM, DROSERA (ROTUNDIFOLIA), HEPAR SULPHURIS CALCAREUM, IPECACUANHA, LACHESIS MUTUS, LOBELIA INFLATA, PHOSPHORUS, PULSATILLA (PRATENSIS), RUMEX CRISPUS, SPONGIA TOSTA) LIQUID [ENERGIQUE, INC.] 2 Current NDC, Legacy NDC, 1 package rows 20241102_a9c72c3a-908a-433b-ba9e-4f525b80ecaa.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 Upper Resp HP CARBO VEGETABILIS, CUPRUM METALLICUM, DROSERA (ROTUNDIFOLIA), HEPAR SULPHURIS CALCAREUM, IPECACUANHA, LACHESIS MUTUS, LOBELIA INFLATA, PHOSPHORUS, PULSATILLA (PRATENSIS), RUMEX CRISPUS, SPONGIA TOSTA Energique, Inc. a9c72c3a-908a-433b-ba9e-4f525b80ecaa 2024-10-31 Warnings Exact identifier ndc (package): 44911-0595-1 ndc (product): 44911-0595 ndc11 (package): 44911059501
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 44911-0595-1 44911059501 30 mL in 1 BOTTLE, DROPPER (44911-0595-1) 30 ml 2021-01-04 0000-00-00 No No Current