Nerve Pro

Product NDC
44911-0495
11-digit product format
449110495
Labeler code
44911
Product ID
44911-0495_c98c29e3-90b3-4b1d-8a1d-83f9a70075c6
Type
HUMAN OTC DRUG
Nonproprietary name
Plantago Major, Xanthoxylum Fraxineum, Colocynthis, Magnesia Phosphorica, Agaricus Muscarius, Hypericum Perforatum, Argentum Nitricum, Carboneum Sulphuratum, Curare, Thallium Metallicum
Dosage form
LIQUID
Route
ORAL
Labeler
Energique, Inc.
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2019-05-14
Substance
AMANITA MUSCARIA FRUITING BODY; CARBON DISULFIDE; CITRULLUS COLOCYNTHIS FRUIT PULP; HYPERICUM PERFORATUM WHOLE; MAGNESIUM PHOSPHATE, DIBASIC TRIHYDRATE; PLANTAGO MAJOR WHOLE; SILVER NITRATE; THALLIUM; TUBOCURARINE CHLORIDE; ZANTHOXYLUM AMERICANUM BARK
Active strength
12; 30; 12; 12; 12; 6; 30; 30; 30; 6 [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
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

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 · 16 matching rows.

View current auxiliary records. · View the auxiliary file history.

Captured / source date, Dataset, Scope table
Captured / source dateDatasetScopePackage NDCSnapshotSource SHA-256
2024-10-04 04:10 UTC · source 2024-10-03excluded productproduct367a005e9d99…383a685ebd0f…
2024-10-04 04:10 UTC · source 2024-10-03excluded packagepackage44911-0495-1367a005e9d99…383a685ebd0f…
2024-07-10 04:00 UTC · source 2024-07-09excluded productproduct557ba5c1ecfa…9c80585c8c6e…
2024-07-10 04:00 UTC · source 2024-07-09excluded packagepackage44911-0495-1557ba5c1ecfa…9c80585c8c6e…
2024-05-28 21:12 UTC · source 2024-05-28excluded productproduct8af77b9d5b6f…d9bbb34c5368…
2024-05-28 21:12 UTC · source 2024-05-28excluded packagepackage44911-0495-18af77b9d5b6f…d9bbb34c5368…
2024-05-15 03:39 UTC · source 2024-05-14excluded productproduct834df4deac94…adcc014656a3…
2024-05-15 03:39 UTC · source 2024-05-14excluded packagepackage44911-0495-1834df4deac94…adcc014656a3…
2024-03-11 06:39 UTC · source 2024-03-08excluded productproduct1332a3947898…d4bfe170f9cd…
2024-03-11 06:39 UTC · source 2024-03-08excluded packagepackage44911-0495-11332a3947898…d4bfe170f9cd…
2022-08-30 03:57 UTC · source 2022-08-29excluded productproductfb8cb913e6d1…eb8c232b6be0…
2022-08-30 03:57 UTC · source 2022-08-29excluded packagepackage44911-0495-1fb8cb913e6d1…eb8c232b6be0…
2022-04-09 23:13 UTC · source 2022-04-08excluded productproduct86f5da6cb304…a595104c45d7…
2022-04-09 23:13 UTC · source 2022-04-08excluded packagepackage44911-0495-186f5da6cb304…a595104c45d7…
2022-04-04 05:40 UTC · source 2022-04-01excluded productproductbd6a592717d7…303034d00443…
2022-04-04 05:40 UTC · source 2022-04-01excluded packagepackage44911-0495-1bd6a592717d7…303034d00443…

Additional Listing Data#

Finished product
Yes
Brand name base
Nerve Pro
Brand name suffix
HP
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
PLANTAGO MAJOR WHOLE12 [hp_X]/mL
ZANTHOXYLUM AMERICANUM BARK30 [hp_X]/mL
CITRULLUS COLOCYNTHIS FRUIT PULP12 [hp_X]/mL
MAGNESIUM PHOSPHATE, DIBASIC TRIHYDRATE12 [hp_X]/mL
AMANITA MUSCARIA FRUITING BODY12 [hp_X]/mL
HYPERICUM PERFORATUM WHOLE6 [hp_X]/mL
SILVER NITRATE30 [hp_X]/mL
CARBON DISULFIDE30 [hp_X]/mL
TUBOCURARINE CHLORIDE30 [hp_X]/mL
THALLIUM6 [hp_X]/mL

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 10 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
W2469WNO6UInternal UNII lookup
A4KL1HMZ7TInternal UNII lookup
23H32AOH17Internal UNII lookup
HF539G9L3QInternal UNII lookup
DIF093I037Internal UNII lookup
XK4IUX8MNBInternal UNII lookup
95IT3W8JZEInternal UNII lookup
S54S8B99E8Internal UNII lookup
900961Z8VRInternal UNII lookup
AD84R52XLFInternal UNII lookup

Harmonized SPL set identifiers#

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

Identifier, FDA.report destination table
IdentifierFDA.report destination
846d5805-6f82-4cb4-b64c-adba6d3004e7Available 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
6cca4355-1206-91f7-02de-17eef38a8622Product name120140508
751c581a-bf64-2fd7-b3ec-ca02c83e4a00Product name120140508
c6b65c52-69c7-df49-550a-a50c137f6218Product name120140508

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
44911-0495-12024-10-29C16284748780-1d6a99b39-49f4-a426-e053-dadaa90af4c2DRUG FACTS:
44911-0495-12022-01-28C16284748780-1d6a99b39-49f4-a426-e053-dadaa90af4c2DRUG FACTS:

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
44911-0495-1Nerve ProHP30 mL in 1 BOTTLE, DROPPERLIQUID303

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
44911-0495NERVE PRO HP (PLANTAGO MAJOR, XANTHOXYLUM FRAXINEUM, COLOCYNTHIS, MAGNESIA PHOSPHORICA, AGARICUS MUSCARIUS, HYPERICUM PERFORATUM, ARGENTUM NITRICUM, CARBONEUM SULPHURATUM, CURARE, THALLIUM METALLICUM) LIQUID [ENERGIQUE, INC.]3Current NDC, Legacy NDC, 1 package rows20241031_846d5805-6f82-4cb4-b64c-adba6d3004e7.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
Nerve Pro HPPLANTAGO MAJOR, XANTHOXYLUM FRAXINEUM, COLOCYNTHIS, MAGNESIA PHOSPHORICA, AGARICUS MUSCARIUS, HYPERICUM PERFORATUM, ARGENTUM NITRICUM, CARBONEUM SULPHURATUM, CURARE, THALLIUM METALLICUMEnergique, Inc.846d5805-6f82-4cb4-b64c-adba6d3004e72024-10-29WarningsExact identifier
ndc (product): 44911-0495

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
44911-0495-14491104950130 mL in 1 BOTTLE, DROPPER (44911-0495-1) 30 ml2019-05-140000-00-00NoNoCurrent