Drosera Combination

Product NDC
63083-9221
Requested package NDC
63083-9221-1
11-digit product format
630839221
Labeler code
63083
Product ID
63083-9221_1d689388-19e7-4ec8-a359-d010c265ff01
Type
HUMAN OTC DRUG
Nonproprietary name
Drosera Combination
Dosage form
LIQUID
Route
ORAL
Labeler
Professional Complementary Health Formulas
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
1984-08-15
Substance
ACTIVATED CHARCOAL; ARSENIC TRIIODIDE; CAUSTICUM; CUPRIC ACETATE; DRIMIA MARITIMA BULB; DROSERA ROTUNDIFOLIA WHOLE; LACHESIS MUTA VENOM; POTASSIUM CARBONATE; PROTORTONIA CACTI
Active strength
12; 6; 6; 6; 6; 6; 12; 12; 4 [hp_X]/29.5mL; [hp_X]/29.5mL; [hp_X]/29.5mL; [hp_X]/29.5mL; [hp_X]/29.5mL; [hp_X]/29.5mL; [hp_X]/29.5mL; [hp_X]/29.5mL; [hp_X]/29.5mL
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…

Additional Listing Data#

Finished product
Yes
Brand name base
Drosera Combination
Brand name suffix
9221
Listing expiration
2027-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
PROTORTONIA CACTI12 [hp_X]/29.5mL
ARSENIC TRIIODIDE6 [hp_X]/29.5mL
CAUSTICUM6 [hp_X]/29.5mL
CUPRIC ACETATE6 [hp_X]/29.5mL
DROSERA ROTUNDIFOLIA WHOLE6 [hp_X]/29.5mL
DRIMIA MARITIMA BULB6 [hp_X]/29.5mL
ACTIVATED CHARCOAL12 [hp_X]/29.5mL
POTASSIUM CARBONATE12 [hp_X]/29.5mL
LACHESIS MUTA VENOM4 [hp_X]/29.5mL

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 9 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
LZB7TFX1LTInternal UNII lookup
3029988O2TInternal UNII lookup
DD5FO1WKFUInternal UNII lookup
39M11XPH03Internal UNII lookup
QR44N9XPJQInternal UNII lookup
3629601H5DInternal UNII lookup
2P3VWU3H10Internal UNII lookup
BQN1B9B9HAInternal UNII lookup
VSW71SS07IInternal UNII lookup

Harmonized SPL set identifiers#

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

Identifier, FDA.report destination table
IdentifierFDA.report destination
5ae94676-2b6e-4888-8691-a8aa9a6c59c9Available on FDA.report

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
63f39a63-5cd1-4016-bd86-2bbb0f6c3139Product name320240506
e5a77e9c-c528-733a-173d-914a234c024bProduct name520240506
0306390c-dd77-4363-afe0-63c58088b2a1Product name120220120
503ea967-4b9c-48cf-9e87-c7975295849dProduct name220220120

FDA-Initiated Inactive NDC Indexing#

Effective, Related label table
EffectiveRelated label
2026-01-08R221
2026-01-08R221
2024-01-30R221
2024-01-30R221

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
63083-9221-1Drosera Combination922129.5 mL in 1 BOTTLE, DROPPERLIQUID29.52

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
63083-9221DROSERA COMBINATION 9221 (DROSERA COMBINATION) LIQUID [PROFESSIONAL COMPLEMENTARY HEALTH FORMULAS]1Current NDC, Legacy NDC, 1 package rows20220210_5ae94676-2b6e-4888-8691-a8aa9a6c59c9.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
Drosera Combination 9221DROSERA COMBINATIONProfessional Complementary Health Formulas5ae94676-2b6e-4888-8691-a8aa9a6c59c92026-01-08WarningsExact identifier
ndc (package): 63083-9221-1
ndc (product): 63083-9221
ndc11 (package): 63083922101

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
63083-9221-16308392210129.5 mL in 1 BOTTLE, DROPPER (63083-9221-1) 29.5 ml1985-08-150000-00-00NoNoCurrent