Numbness HP

Product NDC
44911-0625
11-digit product format
449110625
Labeler code
44911
Product ID
44911-0625_9aec25cf-ef9c-417f-b225-db8a2a20306d
Type
HUMAN OTC DRUG
Nonproprietary name
Aconitum napellus, Agaricus muscarius, Allium cepa, Arnica montana, Coffea cruda, Hypericum perforatum, Lycopodium clavatum, Mercurius solubilis, Phosphorus, Plumbum metallicum
Dosage form
LIQUID
Route
ORAL
Labeler
Energique, Inc.
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2021-05-26
Substance
ACONITUM NAPELLUS WHOLE; AMANITA MUSCARIA FRUITING BODY; ARABICA COFFEE BEAN; ARNICA MONTANA WHOLE; HYPERICUM PERFORATUM WHOLE; LEAD; LYCOPODIUM CLAVATUM SPORE; MERCURIUS SOLUBILIS; ONION; PHOSPHORUS
Active strength
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
Pharmacologic classes
Allergens [CS], Allergens [CS], Cell-mediated Immunity [PE], Cell-mediated Immunity [PE], Dietary Proteins [CS], Dietary Proteins [CS], Increased Histamine Release [PE], Increased Histamine Release [PE], Non-Standardized Food Allergenic Extract [EPC], Non-Standardized Food Allergenic Extract [EPC], Non-Standardized Plant Allergenic Extract [EPC], Plant Proteins [CS], Seed Storage Proteins [CS], Vegetable Proteins [CS]
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Additional Listing Data#

Finished product
Yes
Brand name base
Numbness HP
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
ACONITUM NAPELLUS WHOLE30 [hp_X]/mL
AMANITA MUSCARIA FRUITING BODY30 [hp_X]/mL
ARABICA COFFEE BEAN30 [hp_X]/mL
ARNICA MONTANA WHOLE30 [hp_X]/mL
HYPERICUM PERFORATUM WHOLE30 [hp_X]/mL
LEAD30 [hp_X]/mL
LYCOPODIUM CLAVATUM SPORE30 [hp_X]/mL
MERCURIUS SOLUBILIS30 [hp_X]/mL
ONION30 [hp_X]/mL
PHOSPHORUS30 [hp_X]/mL

Harmonized Identifiers#

Field, Values table
FieldValues
UniiU0NQ8555JD, DIF093I037, 3SW678MX72, O80TY208ZW, XK4IUX8MNB, 2P299V784P, C88X29Y479, 324Y4038G2, 492225Q21H, 27YLU75U4W

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
7792dadb-52b6-46b6-8fdf-80b1171065b5Product name120180810

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
44911-0625-12024-10-29C16284748780-1f386c649-c79b-0266-e053-dadaa90a7c1aDRUG FACTS:
44911-0625-12023-01-30C16284748780-1f386c649-c79b-0266-e053-dadaa90a7c1aDRUG FACTS:

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
44911-0625-1Numbness HP30 mL in 1 BOTTLE, DROPPERLIQUID302

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
44911-0625NUMBNESS HP (ACONITUM NAPELLUS, AGARICUS MUSCARIUS, ALLIUM CEPA, ARNICA MONTANA, COFFEA CRUDA, HYPERICUM PERFORATUM, LYCOPODIUM CLAVATUM, MERCURIUS SOLUBILIS, PHOSPHORUS, PLUMBUM METALLICUM) LIQUID [ENERGIQUE, INC.]2Current NDC, Legacy NDC, 1 package rows20241031_0c4ba547-b4b4-41d0-8a6b-1141ff5f9453.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
44911-0625-14491106250130 mL in 1 BOTTLE, DROPPER (44911-0625-1) 30 ml2021-05-260000-00-00NoNoCurrent