Home NDC 43857-0616-1 Sinusforce
Product NDC 43857-0616
Requested package NDC 43857-0616-1
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 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 · 4 matching rows.
View current auxiliary records. · View the auxiliary file history.
Captured / source date, Snapshot, Source SHA-256 table Captured / source date Snapshot Source SHA-256 2024-07-10 04:00 UTC · source 2024-07-09 557ba5c1ecfa…9c80585c8c6e…2024-05-28 21:12 UTC · source 2024-05-28 8af77b9d5b6f…d9bbb34c5368…2024-05-15 03:39 UTC · source 2024-05-14 834df4deac94…adcc014656a3…2024-03-11 06:39 UTC · source 2024-03-08 1332a3947898…d4bfe170f9cd…
Additional Listing Data#
Finished product Yes
Brand name base Sinusforce
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength ECHINACEA ANGUSTIFOLIA WHOLE 12 [hp_X]/mL NUTMEG 3 [hp_X]/mL FENUGREEK SEED 3 [hp_X]/mL GOLDENSEAL 5 [hp_X]/mL ARSENIC TRIOXIDE 12 [hp_X]/mL POTASSIUM DICHROMATE 30 [hp_X]/mL MERCURIC SULFIDE 3 [hp_X]/mL PULSATILLA VULGARIS WHOLE 12 [hp_X]/mL SEPIA OFFICINALIS JUICE 12 [hp_X]/mL MERCURIUS SOLUBILIS 12 [hp_X]/mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 10 matching rows.
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Product Concepts# FDA-Initiated Inactive NDC Indexing# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 43857-0616-1 Sinusforce 30 mL in 1 BOTTLE, DROPPER LIQUID 30 2
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 43857-0616 SINUSFORCE (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.] 2 Current NDC, Legacy NDC, 1 package rows 20240913_17ceb312-5d0a-4eb0-b1f2-daa6994e1e86.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 Brand Generic Manufacturer SPL set ID Effective date Available safety fields Join Sinusforce ECHINACEA (ANGUSTIFOLIA), NUX MOSCHATA, TRIGONELLA FOENUM GRAECUM, HYDRASTIS CANADENSIS, ARSENICUM ALBUM, KALI BICHROMICUM, MERCURIUS SULPHURATUS RUBER, PULSATILLA (VULGARIS), SEPIA, MERCURIUS SOLUBILIS BioActive Nutritional, Inc. 17ceb312-5d0a-4eb0-b1f2-daa6994e1e86 2024-09-12 Warnings Exact identifier ndc (package): 43857-0616-1 ndc (product): 43857-0616 ndc11 (package): 43857061601
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 43857-0616-1 43857061601 30 mL in 1 BOTTLE, DROPPER (43857-0616-1) 30 ml 2021-09-15 0000-00-00 No No Current