Cough

Product NDC
44911-0319
Requested package NDC
44911-0319-1
11-digit product format
449110319
Labeler code
44911
Product ID
44911-0319_60644aa7-deaf-4ee4-ba57-a0b255a785df
Type
HUMAN OTC DRUG
Nonproprietary name
Arsenicum Album, Bryonia (Alba), Corallium Rubrum, Cuprum Aceticum, Drosera (Rotundifolia), Ipecacuanha, Kali Carbonicum, Phosphorus, Pulsatilla (Pratensis), Spongia Tosta
Dosage form
LIQUID
Route
ORAL
Labeler
Energique, Inc.
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2016-01-12
Substance
ARSENIC TRIOXIDE; BRYONIA ALBA ROOT; CORALLIUM RUBRUM EXOSKELETON; CUPRIC ACETATE; DROSERA ROTUNDIFOLIA WHOLE; IPECAC; PHOSPHORUS; POTASSIUM CARBONATE; PULSATILLA PRATENSIS WHOLE; SPONGIA OFFICINALIS SKELETON, ROASTED
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
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 · 9 matching rows.

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

Captured / source date, Code, Status table
Captured / source dateCodeStatusSnapshotSource SHA-256
2025-08-27 00:01 UTC · source 2025-08-26DDiscontinued by firmf5e01cc5f278…a2eaf40c39c3…
2024-10-04 04:10 UTC · source 2024-10-03IInactivated by FDA367a005e9d99…383a685ebd0f…
2024-07-10 04:00 UTC · source 2024-07-09IInactivated by FDA557ba5c1ecfa…9c80585c8c6e…
2024-05-28 21:12 UTC · source 2024-05-28IInactivated by FDA8af77b9d5b6f…d9bbb34c5368…
2024-05-15 03:39 UTC · source 2024-05-14IInactivated by FDA834df4deac94…adcc014656a3…
2024-03-11 06:39 UTC · source 2024-03-08IInactivated by FDA1332a3947898…d4bfe170f9cd…
2022-08-30 03:57 UTC · source 2022-08-29IInactivated by FDAfb8cb913e6d1…eb8c232b6be0…
2022-04-09 23:13 UTC · source 2022-04-08IInactivated by FDA86f5da6cb304…a595104c45d7…
2022-04-04 05:40 UTC · source 2022-04-01IInactivated by FDAbd6a592717d7…303034d00443…

Additional Listing Data#

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

Active Ingredients#

Ingredient, Strength table
IngredientStrength
ARSENIC TRIOXIDE30 [hp_X]/mL
BRYONIA ALBA ROOT30 [hp_X]/mL
CORALLIUM RUBRUM EXOSKELETON30 [hp_X]/mL
CUPRIC ACETATE30 [hp_X]/mL
DROSERA ROTUNDIFOLIA WHOLE30 [hp_X]/mL
IPECAC30 [hp_X]/mL
POTASSIUM CARBONATE30 [hp_X]/mL
PHOSPHORUS30 [hp_X]/mL
PULSATILLA PRATENSIS WHOLE30 [hp_X]/mL
SPONGIA OFFICINALIS SKELETON, ROASTED30 [hp_X]/mL

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 10 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
S7V92P67HOInternal UNII lookup
T7J046YI2BInternal UNII lookup
2CA71K0DLEInternal UNII lookup
39M11XPH03Internal UNII lookup
QR44N9XPJQInternal UNII lookup
62I3C8233LInternal UNII lookup
BQN1B9B9HAInternal UNII lookup
27YLU75U4WInternal UNII lookup
8E272251DIInternal UNII lookup
1PIP394IIDInternal UNII lookup

Harmonized SPL set identifiers#

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

Identifier, FDA.report destination table
IdentifierFDA.report destination
0c622637-22ce-4124-9440-c10ec42713ffAvailable on FDA.report

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
63f39a63-5cd1-4016-bd86-2bbb0f6c3139Product name320240506
e5a77e9c-c528-733a-173d-914a234c024bProduct name520240506
0306390c-dd77-4363-afe0-63c58088b2a1Product name120220120
503ea967-4b9c-48cf-9e87-c7975295849dProduct name220220120
7792dadb-52b6-46b6-8fdf-80b1171065b5Product name120180810

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
44911-0319-12024-10-24C16284748780-1d6a99b39-ef04-a426-e053-dadaa90af4c2DRUG FACTS:
44911-0319-12022-01-28C16284748780-1d6a99b39-ef04-a426-e053-dadaa90af4c2DRUG FACTS:

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
44911-0319-1CoughHP30 mL in 1 BOTTLE, DROPPERLIQUID306

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
44911-0319COUGH HP (ARSENICUM ALBUM, BRYONIA (ALBA), CORALLIUM RUBRUM, CUPRUM ACETICUM, DROSERA (ROTUNDIFOLIA), IPECACUANHA, KALI CARBONICUM, PHOSPHORUS, PULSATILLA (PRATENSIS), SPONGIA TOSTA) LIQUID [ENERGIQUE, INC.]5Current NDC, Legacy NDC, 1 package rows20250521_0c622637-22ce-4124-9440-c10ec42713ff.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
Cough HPARSENICUM ALBUM, BRYONIA (ALBA), CORALLIUM RUBRUM, CUPRUM ACETICUM, DROSERA (ROTUNDIFOLIA), IPECACUANHA, KALI CARBONICUM, PHOSPHORUS, PULSATILLA (PRATENSIS), SPONGIA TOSTAEnergique, Inc.0c622637-22ce-4124-9440-c10ec42713ff2025-11-24WarningsExact identifier
ndc (package): 44911-0319-1
ndc (product): 44911-0319
ndc11 (package): 44911031901

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
44911-0319-14491103190130 mL in 1 BOTTLE, DROPPER (44911-0319-1) 30 ml2016-01-120000-00-00NoNoCurrent