Allergy Nosode

Product NDC
63083-4017
Requested package NDC
63083-4017-2
11-digit product format
630834017
Labeler code
63083
Product ID
63083-4017_8f6adf24-31cc-4860-b955-0076730f68ba
Type
HUMAN OTC DRUG
Nonproprietary name
Allergy Nosode
Dosage form
LIQUID
Route
ORAL
Labeler
Professional Complementary Health Formulas
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
1984-08-15
Substance
HOUSE DUST; STACHYBOTRYS CHARTARUM; MEDICAGO SATIVA WHOLE; FRAXINUS LATIFOLIA WHOLE; TARAXACUM OFFICINALE; POTASSIUM DICHROMATE; CALCIUM SULFIDE; HISTAMINE; SILICON DIOXIDE; GUAIAC; LUFFA OPERCULATA FRUIT
Active strength
12; 12; 12; 12; 12; 30; 12; 12; 12; 6; 6 [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL
Pharmacologic classes
Allergens [CS], Allergens [CS], Cell-mediated Immunity [PE], Cell-mediated Immunity [PE], Fungal Proteins [CS], House Dust [CS], Increased Histamine Release [PE], Increased Histamine Release [PE], Increased IgG Production [PE], Increased IgG Production [PE], Non-Standardized Fungal Allergenic Extract [EPC], Non-Standardized House Dust Allergenic Extract [EPC]
NDC exclude flag
No
Listing certified through
2027-12-31
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 · 15 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…
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…

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.

Additional Listing Data#

Finished product
Yes
Brand name base
Allergy Nosode
Brand name suffix
4017
Listing expiration
2027-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
HOUSE DUST12 [hp_X]/59mL
STACHYBOTRYS CHARTARUM12 [hp_X]/59mL
MEDICAGO SATIVA WHOLE12 [hp_X]/59mL
FRAXINUS LATIFOLIA WHOLE12 [hp_X]/59mL
TARAXACUM OFFICINALE12 [hp_X]/59mL
POTASSIUM DICHROMATE30 [hp_X]/59mL
CALCIUM SULFIDE12 [hp_X]/59mL
HISTAMINE12 [hp_X]/59mL
SILICON DIOXIDE12 [hp_X]/59mL
GUAIAC6 [hp_X]/59mL
LUFFA OPERCULATA FRUIT6 [hp_X]/59mL

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 11 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
EYO007VX98Internal UNII lookup
HJ4L70T1ZPInternal UNII lookup
DJO934BRBDInternal UNII lookup
024W88F557Internal UNII lookup
39981FM375Internal UNII lookup
T4423S18FMInternal UNII lookup
1MBW07J51QInternal UNII lookup
820484N8I3Internal UNII lookup
ETJ7Z6XBU4Internal UNII lookup
03C8A0DFJ8Internal UNII lookup
C4MO6809HUInternal UNII lookup

Harmonized SPL set identifiers#

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

Identifier, FDA.report destination table
IdentifierFDA.report destination
da9145a5-42e9-4dba-9d11-195848e628a4Available on FDA.report

FDA-Initiated Inactive NDC Indexing#

Effective, Related label table
EffectiveRelated label
2026-01-09N17
2026-01-09N17
2024-01-30N17
2024-01-30N17

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
63083-4017-2Allergy Nosode401759 mL in 1 BOTTLE, DROPPERLIQUID592

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
63083-4017ALLERGY NOSODE 4017 (ALLERGY NOSODE) LIQUID [PROFESSIONAL COMPLEMENTARY HEALTH FORMULAS]1Current NDC, Legacy NDC, 1 package rows20220301_da9145a5-42e9-4dba-9d11-195848e628a4.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
Allergy Nosode 4017ALLERGY NOSODEProfessional Complementary Health Formulasda9145a5-42e9-4dba-9d11-195848e628a42026-01-08WarningsExact identifier
ndc (package): 63083-4017-2
ndc (product): 63083-4017
ndc11 (package): 63083401702

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
63083-4017-26308340170259 mL in 1 BOTTLE, DROPPER (63083-4017-2) 59 ml1985-08-150000-00-00NoNoCurrent