D-139

Product NDC
58264-0163
11-digit product format
582640163
Labeler code
58264
Product ID
58264-0163_2b9f0ae7-5ebc-31e5-e063-6294a90a6ebf
Type
HUMAN OTC DRUG
Nonproprietary name
Arsenicum album, Belladonna, Calcarea carbonica, Carbo vegetabilis, Ferrum phosphoricum, Lycopodium, Natrum phosphoricum, Nux vomica, Phosphorus, Pulsatilla, Hydrastis
Dosage form
SOLUTION
Route
SUBLINGUAL
Labeler
DNA Labs, Inc.
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2022-09-08
Substance
ANEMONE PRATENSIS; LYCOPODIUM CLAVATUM SPORE; PHOSPHORUS; FERROSOFERRIC PHOSPHATE; ARSENIC TRIIODIDE; ATROPA BELLADONNA; SODIUM PHOSPHATE, DIBASIC, HEPTAHYDRATE; ACTIVATED CHARCOAL; OYSTER SHELL CALCIUM CARBONATE, CRUDE; GOLDENSEAL; STRYCHNOS NUX-VOMICA SEED
Active strength
6; 6; 6; 6; 6; 6; 6; 6; 6; 3; 6 [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; [hp_X]/mL
Pharmacologic classes
Allergens [CS], Cell-mediated Immunity [PE], Increased Histamine Release [PE], Increased IgG Production [PE], 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 · 2 matching rows.

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

Captured / source date, Dataset, Scope table
Captured / source dateDatasetScopeProduct NDCPackage NDCCodeStatusReporting periodArchiveSnapshotSource SHA-256
2025-01-11 03:41 UTC · source 2025-01-10excluded productproduct58264-0163UExcluded because listing certification expiredexcluded / ndc_excluded.zip0efc9e666f02…f202fb6c5f17…
2025-01-11 03:41 UTC · source 2025-01-10excluded packagepackage58264-016358264-0163-1UExcluded because listing certification expiredexcluded / ndc_excluded.zip0efc9e666f02…f202fb6c5f17…

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
D-139
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
ANEMONE PRATENSIS6 [hp_X]/mL
LYCOPODIUM CLAVATUM SPORE6 [hp_X]/mL
PHOSPHORUS6 [hp_X]/mL
FERROSOFERRIC PHOSPHATE6 [hp_X]/mL
ARSENIC TRIIODIDE6 [hp_X]/mL
ATROPA BELLADONNA6 [hp_X]/mL
SODIUM PHOSPHATE, DIBASIC, HEPTAHYDRATE6 [hp_X]/mL
ACTIVATED CHARCOAL6 [hp_X]/mL
OYSTER SHELL CALCIUM CARBONATE, CRUDE6 [hp_X]/mL
GOLDENSEAL3 [hp_X]/mL
STRYCHNOS NUX-VOMICA SEED6 [hp_X]/mL

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 11 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
8E272251DIInternal UNII lookup
C88X29Y479Internal UNII lookup
27YLU75U4WInternal UNII lookup
91GQH8I5F7Internal UNII lookup
3029988O2TInternal UNII lookup
WQZ3G9PF0HInternal UNII lookup
70WT22SF4BInternal UNII lookup
2P3VWU3H10Internal UNII lookup
2E32821G6IInternal UNII lookup
ZW3Z11D0JVInternal UNII lookup
269XH13919Internal UNII lookup

Harmonized SPL set identifiers#

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

Identifier, FDA.report destination table
IdentifierFDA.report destination
e830774e-35c8-7309-e053-2995a90ae043Available on FDA.report

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
efd58dcf-540a-4531-8766-e713129ca6f2Product name120250307
4b7700e3-6e0e-45e5-9d22-6f754d61386eProduct name220250304
726062af-1135-4707-a1d7-57256991bbf9Product name220250226
63f39a63-5cd1-4016-bd86-2bbb0f6c3139Product name320240506
e5a77e9c-c528-733a-173d-914a234c024bProduct name520240506
7cda52fc-125f-421c-8fea-bc1974370c49Product name220180703
0ca1d589-929b-4b33-bc5b-1d84abdafa6aProduct name120150324
fc363c46-397b-4476-ac0f-70e43e8e4592Product name120150324
19c71a3d-ed9c-166b-a7e5-38c250c35631Product name120140508

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
58264-0163-1D-13929.57 mL in 1 BOTTLE, GLASSSOLUTION29.572

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
58264-0163D-139 (ARSENICUM ALBUM, BELLADONNA, CALCAREA CARBONICA, CARBO VEGETABILIS, FERRUM PHOSPHORICUM, LYCOPODIUM, NATRUM PHOSPHORICUM, NUX VOMICA, PHOSPHORUS, PULSATILLA, HYDRASTIS) SOLUTION [DNA LABS, INC.]2Current NDC, Legacy NDC, 1 package rows20250115_e830774e-35c8-7309-e053-2995a90ae043.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
D-139ARSENICUM ALBUM, BELLADONNA, CALCAREA CARBONICA, CARBO VEGETABILIS, FERRUM PHOSPHORICUM, LYCOPODIUM, NATRUM PHOSPHORICUM, NUX VOMICA, PHOSPHORUS, PULSATILLA, HYDRASTISDNA Labs, Inc.e830774e-35c8-7309-e053-2995a90ae0432025-01-13WarningsExact identifier
ndc (product): 58264-0163

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
58264-0163-15826401630129.57 mL in 1 BOTTLE, GLASS (58264-0163-1) 29.57 ml2022-09-080000-00-00NoNoCurrent