Apizelen

Product NDC
43857-0490
Requested package NDC
43857-0490-1
11-digit product format
438570490
Labeler code
43857
Product ID
43857-0490_abb9e2e2-ae38-48f8-8e97-3e9e23caabc4
Type
HUMAN OTC DRUG
Nonproprietary name
Alfalfa, Aralia Quinquefolia, Avena Sativa, Beta Vulgaris, Calendula Officinalis, Chelidonium Majus, Echinacea (Angustifolia), Natrum Muriaticum, Oxalis Acetosella, Paloondo, Phytolacca Decandra, Trifolium Pratense, Urtica Dioica, Viscum Album, Cobalt Acetate, Cobalt Gluconate, Copper Gluconate, Cuprum Aceticum, Glutathione, Magnesium Gluconicum Dihydricum, Ganoderma Lucidum, Ubidecarenonum, Argentum Metallicum, Germanium Metallicum
Dosage form
LIQUID
Route
ORAL
Labeler
BioActive Nutritional, Inc.
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2018-09-10
Marketing end
0000-00-00
Substance
ALFALFA; AMERICAN GINSENG; AVENA SATIVA FLOWERING TOP; BETA VULGARIS; CALENDULA OFFICINALIS FLOWERING TOP; CHELIDONIUM MAJUS; ECHINACEA ANGUSTIFOLIA; SODIUM CHLORIDE; OXALIS ACETOSELLA LEAF; LARREA TRIDENTATA LEAF; PHYTOLACCA AMERICANA ROOT; TRIFOLIUM PRATENSE FLOWER; URTICA DIOICA; VISCUM ALBUM FRUITING TOP; COBALTOUS ACETATE; COBALTOUS GLUCONATE; COPPER GLUCONATE; CUPRIC ACETATE; GLUTATHIONE; MAGNESIUM GLUCONATE; REISHI; UBIDECARENONE; SILVER; GERMANIUM
Active strength
2 [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL
NDC exclude flag
No
Listing certified through
2020-12-31
Current FDA listing
Historical FDA.report record

NDC auxiliary status#

These records are reproduced from FDA’s unfinished, excluded, and compounder listings. They describe what appeared in the source files; a missing record does not establish a regulatory status. View all current auxiliary records, including entries without an NDC. · View the auxiliary file history.

Current NDC status page 1 of 1 · 1 matching rows.

Dataset, Scope, Product NDC table
DatasetScopeProduct NDCPackage NDCCodeStatusReporting periodSource date
excluded packagepackage43857-049043857-0490-1DDiscontinued by firm2026-08-03

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 · 11 matching rows.

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

Captured / source date, Snapshot, Source SHA-256 table
Captured / source dateSnapshotSource SHA-256
2025-12-14 17:58 UTC · source 2025-12-05d630ba8d3edf…732f749b63fb…
2025-08-27 00:01 UTC · source 2025-08-26f5e01cc5f278…a2eaf40c39c3…
2025-04-01 02:39 UTC · source 2025-03-312ef7874e63bc…57b86245f4fa…
2025-03-28 20:22 UTC · source 2025-03-28a1b67e2a42f9…c4cf2c586c0d…
2025-03-22 03:12 UTC · source 2025-03-21cfe11265f3b6…090c488252e2…
2025-03-10 12:48 UTC · source 2025-03-10cdf11ea48f46…ba0047e9e063…
2025-02-02 03:52 UTC · source 2025-01-31302b2466d912…e7b80fea0513…
2025-01-20 13:05 UTC · source 2025-01-20ed331223b511…672a5bd82f5f…
2025-01-11 03:41 UTC · source 2025-01-100efc9e666f02…f202fb6c5f17…
2024-11-09 02:27 UTC · source 2024-11-08ad56d346431e…cc804d4bbf1e…
2024-10-04 04:10 UTC · source 2024-10-03367a005e9d99…383a685ebd0f…

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
43857-0490-14385704900130 mL in 1 BOTTLE, DROPPER (43857-0490-1) 30 ml2018-09-100000-00-00NoNoCurrent