FDA.reportPublic FDA data

Sinusforce

Product NDC
43857-0616
11-digit product format
438570616
Labeler code
43857
Product ID
43857-0616_e347705f-1a25-4e61-a867-5328fefc3de4
Type
HUMAN OTC DRUG
Nonproprietary name
Echinacea (Angustifolia), Nux Moschata, Trigonella Foenum Graecum, Hydrastis Canadensis, Arsenicum Album, Kali Bichromicum, Mercurius Sulphuratus Ruber, Pulsatilla (Vulgaris), Sepia, Mercurius Solubilis
Dosage form
LIQUID
Route
ORAL
Labeler
BioActive Nutritional, Inc.
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2021-09-15
Substance
ARSENIC TRIOXIDE; ECHINACEA ANGUSTIFOLIA WHOLE; FENUGREEK SEED; GOLDENSEAL; MERCURIC SULFIDE; MERCURIUS SOLUBILIS; NUTMEG; POTASSIUM DICHROMATE; PULSATILLA VULGARIS WHOLE; SEPIA OFFICINALIS JUICE
Active strength
12; 3; 3; 5; 12; 30; 3; 12; 12; 12 [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], Cell-mediated Immunity [PE], Dietary Proteins [CS], Food Additives [CS], Increased Histamine Release [PE], Non-Standardized Food Allergenic Extract [EPC], Non-Standardized Plant Allergenic Extract [EPC], Plant Proteins [CS], Seed Storage 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
Sinusforce
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
ARSENIC TRIOXIDE12 [hp_X]/mL
ECHINACEA ANGUSTIFOLIA WHOLE3 [hp_X]/mL
FENUGREEK SEED3 [hp_X]/mL
GOLDENSEAL5 [hp_X]/mL
MERCURIC SULFIDE12 [hp_X]/mL
MERCURIUS SOLUBILIS30 [hp_X]/mL
NUTMEG3 [hp_X]/mL
POTASSIUM DICHROMATE12 [hp_X]/mL
PULSATILLA VULGARIS WHOLE12 [hp_X]/mL
SEPIA OFFICINALIS JUICE12 [hp_X]/mL

Harmonized Identifiers#

Field, Values table
FieldValues
UniiS7V92P67HO, VB06AV5US8, 654825W09Z, ZW3Z11D0JV, ZI0T668SF1, 324Y4038G2, AEE24M3MQ9, T4423S18FM, I76KB35JEV, QDL83WN8C2

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
63f39a63-5cd1-4016-bd86-2bbb0f6c3139Product name320240506
e5a77e9c-c528-733a-173d-914a234c024bProduct name520240506

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
43857-0616-12024-09-12C16284748780-1f386c649-edcc-0266-e053-dadaa90a7c1aDRUG FACTS:
43857-0616-12023-01-30C16284748780-1f386c649-edcc-0266-e053-dadaa90a7c1aDRUG FACTS:

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
43857-0616-1Sinusforce30 mL in 1 BOTTLE, DROPPERLIQUID302

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
43857-0616SINUSFORCE (ECHINACEA (ANGUSTIFOLIA), NUX MOSCHATA, TRIGONELLA FOENUM GRAECUM, HYDRASTIS CANADENSIS, ARSENICUM ALBUM, KALI BICHROMICUM, MERCURIUS SULPHURATUS RUBER, PULSATILLA (VULGARIS), SEPIA, MERCURIUS SOLUBILIS) LIQUID [BIOACTIVE NUTRITIONAL, INC.]2Current NDC, Legacy NDC, 1 package rows20240913_17ceb312-5d0a-4eb0-b1f2-daa6994e1e86.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
43857-0616-14385706160130 mL in 1 BOTTLE, DROPPER (43857-0616-1) 30 ml2021-09-150000-00-00NoNoCurrent