FDA.reportPublic FDA data

Parathyropar

Product NDC
44911-0370
Requested package NDC
44911-0370-1
11-digit product format
449110370
Labeler code
44911
Product ID
44911-0370_00acd718-6e5e-40aa-93ed-ae6a60a5c4f0
Type
HUMAN OTC DRUG
Nonproprietary name
Symphytum Officinale, Baryta Carbonica, Calcarea Carbonica, Calcarea Phosphorica, Hekla Lava, Manganum Metallicum, Rhus Tox, Silicea, Parathormonum
Dosage form
LIQUID
Route
ORAL
Labeler
Energique, Inc.
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2016-06-16
Marketing end
2027-02-21
Substance
BARIUM CARBONATE; COMFREY ROOT; HEKLA LAVA; MANGANESE; OYSTER SHELL CALCIUM CARBONATE, CRUDE; PARATHYROID HORMONE; SILICON DIOXIDE; TOXICODENDRON PUBESCENS LEAF; TRIBASIC CALCIUM PHOSPHATE
Active strength
12; 6; 12; 12; 12; 6; 12; 12; 12 [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_C]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL
Pharmacologic classes
Blood Coagulation Factor [EPC], Calcium [CS], Cations, Divalent [CS], Increased Coagulation Factor Activity [PE], Parathyroid Hormone [CS], Parathyroid Hormone [EPC], Phosphate Binder [EPC], Phosphate Chelating Activity [MoA]
NDC exclude flag
No
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 dateSnapshotSource SHA-256
2024-10-04 04:10 UTC · source 2024-10-03367a005e9d99…383a685ebd0f…
2024-07-10 04:00 UTC · source 2024-07-09557ba5c1ecfa…9c80585c8c6e…
2024-05-28 21:12 UTC · source 2024-05-288af77b9d5b6f…d9bbb34c5368…
2024-05-15 03:39 UTC · source 2024-05-14834df4deac94…adcc014656a3…
2024-03-11 06:39 UTC · source 2024-03-081332a3947898…d4bfe170f9cd…

Additional Listing Data#

Finished product
Yes
Brand name base
Parathyropar

Active Ingredients#

Ingredient, Strength table
IngredientStrength
COMFREY ROOT6 [hp_X]/mL
BARIUM CARBONATE12 [hp_X]/mL
OYSTER SHELL CALCIUM CARBONATE, CRUDE12 [hp_X]/mL
TRIBASIC CALCIUM PHOSPHATE12 [hp_X]/mL
HEKLA LAVA12 [hp_X]/mL
MANGANESE12 [hp_X]/mL
TOXICODENDRON PUBESCENS LEAF12 [hp_X]/mL
SILICON DIOXIDE12 [hp_X]/mL
PARATHYROID HORMONE6 [hp_C]/mL

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 9 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
M9VVZ08EKQInternal UNII lookup
6P669D8HQ8Internal UNII lookup
2E32821G6IInternal UNII lookup
91D9GV0Z28Internal UNII lookup
C21158IIRKInternal UNII lookup
42Z2K6ZL8PInternal UNII lookup
6IO182RP7AInternal UNII lookup
ETJ7Z6XBU4Internal UNII lookup
N19A0T0E5JInternal UNII lookup

Harmonized SPL set identifiers#

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

Identifier, FDA.report destination table
IdentifierFDA.report destination
bd13617a-c470-4421-8f47-43a98036f40bAvailable on FDA.report

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
bee4fa8d-8d82-423a-a0b5-40a89dd13a99Product name120250618
e0d2eb29-08bd-4bba-90d1-c91c68a38767Product name420250516
30b0ac6e-02aa-0e5c-0d8b-cffdf3a282b2Product name520250304
334fe8d2-68fb-4331-a576-420e302ec069Product name720240320
444b3e50-f226-46ef-bfca-2e7035d140cdProduct name120190611
e92765c1-be81-432a-b909-1b10777ec378Product name120190208
7cda52fc-125f-421c-8fea-bc1974370c49Product name220180703
d5e51f11-ad28-caa4-4b49-4143974782adProduct name120150831
0ca1d589-929b-4b33-bc5b-1d84abdafa6aProduct name120150324
fc363c46-397b-4476-ac0f-70e43e8e4592Product name120150324
a0139244-df6d-41aa-899a-9c06b76d61f2Product name120150318
0441a8f5-3835-497c-aedd-bc78cba56b2aProduct name120150317
87711080-88eb-65c5-b2dd-bf99e700a372Product name120140508
ec2149b3-5c6d-5344-f757-c86411073075Product name120140508

FDA-Initiated Inactive NDC Indexing#

Effective, Related label table
EffectiveRelated label
2024-10-29DRUG FACTS:
2024-10-29DRUG FACTS:
2024-01-30DRUG FACTS:
2024-01-30DRUG FACTS:
2022-02-21DRUG FACTS:
2022-02-21DRUG FACTS:
2022-01-28DRUG FACTS:
2022-01-28DRUG FACTS:

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
44911-0370-1Parathyropar30 mL in 1 BOTTLE, DROPPERLIQUID307

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
44911-0370PARATHYROPAR (SYMPHYTUM OFFICINALE, BARYTA CARBONICA, CALCAREA CARBONICA, CALCAREA PHOSPHORICA, HEKLA LAVA, MANGANUM METALLICUM, RHUS TOX, SILICEA, PARATHORMONUM) LIQUID [ENERGIQUE, INC.]6Current NDC, Legacy NDC, 1 package rows20241031_bd13617a-c470-4421-8f47-43a98036f40b.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
ParathyroparSYMPHYTUM OFFICINALE, BARYTA CARBONICA, CALCAREA CARBONICA, CALCAREA PHOSPHORICA, HEKLA LAVA, MANGANUM METALLICUM, RHUS TOX, SILICEA, PARATHORMONUMEnergique, Inc.bd13617a-c470-4421-8f47-43a98036f40b2025-10-06WarningsExact identifier
ndc (package): 44911-0370-1
ndc (product): 44911-0370
ndc11 (package): 44911037001

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
44911-0370-14491103700130 mL in 1 BOTTLE, DROPPER (44911-0370-1) 30 ml2016-06-162027-02-21NoNoCurrent