Back and Leg HP

Product NDC
44911-0624
11-digit product format
449110624
Labeler code
44911
Product ID
44911-0624_7561e824-ceb3-4d2c-8090-748a858daf10
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Aconitum Napellus, Aesculus Hippocastanum, Colocynthis, Gnaphalium Polycephalum, Hypericum Perforatum, Magnesia Phosphorica, Plumbum Metallicum, Rhus Tox, Arnica Montana
Dosage form
LIQUID
Route
ORAL
Labeler
Energique, Inc.
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2021-05-27
Substance
ACONITUM NAPELLUS WHOLE; ARNICA MONTANA WHOLE; CITRULLUS COLOCYNTHIS FRUIT PULP; HORSE CHESTNUT; HYPERICUM PERFORATUM WHOLE; LEAD; MAGNESIUM PHOSPHATE, DIBASIC TRIHYDRATE; PSEUDOGNAPHALIUM OBTUSIFOLIUM WHOLE; TOXICODENDRON PUBESCENS LEAF
Active strength
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
Pharmacologic classes
Calculi Dissolution Agent [EPC], Increased Large Intestinal Motility [PE], Inhibition Large Intestine Fluid/Electrolyte Absorption [PE], Inhibition Small Intestine Fluid/Electrolyte Absorption [PE], Magnesium Ion Exchange Activity [MoA], Osmotic Activity [MoA], Osmotic Laxative [EPC], Stimulation Large Intestine Fluid/Electrolyte Secretion [PE]
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Additional Listing Data#

Finished product
Yes
Brand name base
Back and Leg HP
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
ACONITUM NAPELLUS WHOLE30 [hp_X]/mL
HORSE CHESTNUT30 [hp_X]/mL
CITRULLUS COLOCYNTHIS FRUIT PULP30 [hp_X]/mL
PSEUDOGNAPHALIUM OBTUSIFOLIUM WHOLE30 [hp_X]/mL
HYPERICUM PERFORATUM WHOLE30 [hp_X]/mL
MAGNESIUM PHOSPHATE, DIBASIC TRIHYDRATE30 [hp_X]/mL
LEAD30 [hp_X]/mL
TOXICODENDRON PUBESCENS LEAF30 [hp_X]/mL
ARNICA MONTANA WHOLE30 [hp_X]/mL

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 9 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
U0NQ8555JDInternal UNII lookup
3C18L6RJAZInternal UNII lookup
23H32AOH17Internal UNII lookup
36XQ854NWWInternal UNII lookup
XK4IUX8MNBInternal UNII lookup
HF539G9L3QInternal UNII lookup
2P299V784PInternal UNII lookup
6IO182RP7AInternal UNII lookup
O80TY208ZWInternal UNII lookup

Harmonized SPL set identifiers#

SPL set identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
45f8cdd2-d518-453a-8aa4-a0cb6b4e6eb0Available on FDA.report

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
6e3c022f-0786-43f1-8857-edff89d5153fProduct name120260309
95250459-30e4-45c1-b08a-993044f49109Product name220250805
efd58652-cb8f-4018-91ca-4b0eb2ff729fProduct name720240226
362d7abb-94e6-4c60-9a58-266894157713Product name120231023
e2db08c6-133f-4f4f-afb4-e90a2418d6f6Product name120230320
6bd95106-a412-1dad-b9cc-4cb74bfb27ceProduct name220230315
9badc7be-250a-44ab-aa36-926af3f02679Product name120210527
2641ccb3-721d-4fbf-9f2f-ca2f18157a62Product name320210309
11ed6f83-cdd2-4637-8379-b1a1d3ae3cdeProduct name120181101
7cda52fc-125f-421c-8fea-bc1974370c49Product name220180703
86c45a79-b9f0-4476-a27c-6e10db098497Product name120180125
26acd337-b838-40ac-bcbc-05c3b81c8712Product name120170323
d5e51f11-ad28-caa4-4b49-4143974782adProduct name120150831
290f523a-f9db-9774-b5a9-e1f908ac1782Product name120150828
e7e58cd3-cacb-49df-8d34-1ee335614abbProduct name120150609
0ca1d589-929b-4b33-bc5b-1d84abdafa6aProduct name120150324
fc363c46-397b-4476-ac0f-70e43e8e4592Product name120150324
c6b65c52-69c7-df49-550a-a50c137f6218Product name120140508

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
44911-0624-12023-11-30C16284748780-1f386c649-e951-0266-e053-dadaa90a7c1aDRUG FACTS:
44911-0624-12023-01-30C16284748780-1f386c649-e951-0266-e053-dadaa90a7c1aDRUG FACTS:

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
44911-0624-1Back and Leg HP30 mL in 1 BOTTLE, DROPPERLIQUID302

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
44911-0624BACK AND LEG HP (ACONITUM NAPELLUS, AESCULUS HIPPOCASTANUM, COLOCYNTHIS, GNAPHALIUM POLYCEPHALUM, HYPERICUM PERFORATUM, MAGNESIA PHOSPHORICA, PLUMBUM METALLICUM, RHUS TOX, ARNICA MONTANA) LIQUID [ENERGIQUE, INC.]2Current NDC, Legacy NDC, 1 package rows20231201_45f8cdd2-d518-453a-8aa4-a0cb6b4e6eb0.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
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Back and Leg HPACONITUM NAPELLUS, AESCULUS HIPPOCASTANUM, COLOCYNTHIS, GNAPHALIUM POLYCEPHALUM, HYPERICUM PERFORATUM, MAGNESIA PHOSPHORICA, PLUMBUM METALLICUM, RHUS TOX, ARNICA MONTANAEnergique, Inc.45f8cdd2-d518-453a-8aa4-a0cb6b4e6eb02023-11-30WarningsExact identifier
ndc (product): 44911-0624

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
44911-0624-14491106240130 mL in 1 BOTTLE, DROPPER (44911-0624-1) 30 ml2021-05-270000-00-00NoNoCurrent