D-24

Product NDC
58264-0024
Requested package NDC
58264-0024-1
11-digit product format
582640024
Labeler code
58264
Product ID
58264-0024_2b9ea4e9-9a50-adab-e063-6394a90a8323
Type
HUMAN OTC DRUG
Nonproprietary name
BRYONIA ALBA ROOT, RANUNCULUS BULBOSUS, CITRULLUS COLOCYNTHIS FRUIT PULP, BLACK COHOSH, SODIUM SULFATE ANHYDROUS, and POTASSIUM CARBONATE
Dosage form
SOLUTION/ DROPS
Route
SUBLINGUAL
Labeler
DNA Labs, Inc.
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
1990-01-01
Substance
BRYONIA ALBA ROOT; RANUNCULUS BULBOSUS; CITRULLUS COLOCYNTHIS FRUIT PULP; BLACK COHOSH; SODIUM SULFATE ANHYDROUS; POTASSIUM CARBONATE
Active strength
4; 4; 8; 6; 6; 6 [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL
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 · 6 matching rows.

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

Captured / source date, Code, Status table
Captured / source dateCodeStatusSnapshotSource SHA-256
2025-01-11 03:41 UTC · source 2025-01-10UExcluded because listing certification expired0efc9e666f02…f202fb6c5f17…
2022-04-09 23:13 UTC · source 2022-04-08IInactivated by FDA86f5da6cb304…a595104c45d7…
2022-04-04 05:40 UTC · source 2022-04-01IInactivated by FDAbd6a592717d7…303034d00443…
2021-12-27 23:28 UTC · source 2021-12-27IInactivated by FDA8dfbde2a14a4…c9ff85d89658…
2020-12-18 03:04 UTC · source 2020-12-17IInactivated by FDAe2bbac7714bc…27bdfed8d636…
2020-06-10 20:45 UTC · source 2020-06-10IInactivated by FDA9bebd1f3094a…5416666fcb17…

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-24
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
BRYONIA ALBA ROOT4 [hp_X]/mL
RANUNCULUS BULBOSUS4 [hp_X]/mL
CITRULLUS COLOCYNTHIS FRUIT PULP8 [hp_X]/mL
BLACK COHOSH6 [hp_X]/mL
SODIUM SULFATE ANHYDROUS6 [hp_X]/mL
POTASSIUM CARBONATE6 [hp_X]/mL

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 6 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
T7J046YI2BInternal UNII lookup
AEQ8NXJ0MBInternal UNII lookup
23H32AOH17Internal UNII lookup
K73E24S6X9Internal UNII lookup
36KCS0R750Internal UNII lookup
BQN1B9B9HAInternal UNII lookup

Harmonized SPL set identifiers#

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

Identifier, FDA.report destination table
IdentifierFDA.report destination
4247e932-d5e6-4465-ae82-763dbf43d7ebAvailable on FDA.report

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
95250459-30e4-45c1-b08a-993044f49109Product name220250805
362d7abb-94e6-4c60-9a58-266894157713Product name120231023
9badc7be-250a-44ab-aa36-926af3f02679Product name120210527
816b97af-edc5-4060-aff1-b814bdbcad50Product name120190415
26acd337-b838-40ac-bcbc-05c3b81c8712Product name120170323

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
58264-0024-12022-06-02C16284748780-19d75b9d0-50e0-f424-e053-dadaa90a57ceD-24
58264-0024-12020-01-31C16284748780-19d75b9d0-50e0-f424-e053-dadaa90a57ceD-24

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
58264-0024-1D-2429.57 mL in 1 BOTTLE, GLASSSOLUTION/ DROPS29.573

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
58264-0024D-24 (BRYONIA ALBA ROOT, RANUNCULUS BULBOSUS, CITRULLUS COLOCYNTHIS FRUIT PULP, BLACK COHOSH, SODIUM SULFATE ANHYDROUS, AND POTASSIUM CARBONATE) SOLUTION/ DROPS [DNA LABS, INC.]3Current NDC, Legacy NDC, 1 package rows20250115_4247e932-d5e6-4465-ae82-763dbf43d7eb.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-24BRYONIA ALBA ROOT, RANUNCULUS BULBOSUS, CITRULLUS COLOCYNTHIS FRUIT PULP, BLACK COHOSH, SODIUM SULFATE ANHYDROUS, AND POTASSIUM CARBONATEDNA Labs, Inc.4247e932-d5e6-4465-ae82-763dbf43d7eb2025-01-13WarningsExact identifier
ndc (package): 58264-0024-1
ndc (product): 58264-0024
ndc11 (package): 58264002401

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
58264-0024-15826400240129.57 mL in 1 BOTTLE, GLASS (58264-0024-1) 29.57 ml1990-01-010000-00-00NoNoCurrent