Adjustment Disorders Formula

Product NDC
63083-2097
Requested package NDC
63083-2097-2
11-digit product format
630832097
Labeler code
63083
Product ID
63083-2097_6da1dc28-d85c-4074-8afe-487f8a8a8c84
Type
HUMAN OTC DRUG
Nonproprietary name
Adjustment Disorders Formula
Dosage form
LIQUID
Route
ORAL
Labeler
Professional Complementary Health Formulas
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
1984-08-15
Substance
DIEFFENBACHIA SEGUINE WHOLE; ANTIPYRINE; ARUNDO PLINIANA ROOT; DIGITALIS; NITROGLYCERIN; XEROPHYLLUM ASPHODELOIDES WHOLE; AGAVE ATROVIRENS TOP; WOOD CREOSOTE; LACHESIS MUTA VENOM; RABIES VIRUS
Active strength
3; 6; 6; 6; 6; 6; 12; 24; 30; 30 [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
Nitrate Vasodilator [EPC], Nitrates [CS], Vasodilation [PE]
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
Adjustment Disorders Formula
Brand name suffix
2097
Listing expiration
2027-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
DIEFFENBACHIA SEGUINE WHOLE3 [hp_X]/59mL
ANTIPYRINE6 [hp_X]/59mL
ARUNDO PLINIANA ROOT6 [hp_X]/59mL
DIGITALIS6 [hp_X]/59mL
NITROGLYCERIN6 [hp_X]/59mL
XEROPHYLLUM ASPHODELOIDES WHOLE6 [hp_X]/59mL
AGAVE ATROVIRENS TOP12 [hp_X]/59mL
WOOD CREOSOTE24 [hp_X]/59mL
LACHESIS MUTA VENOM30 [hp_X]/59mL
RABIES VIRUS30 [hp_X]/59mL

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 10 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
01800C6E6BInternal UNII lookup
T3CHA1B51HInternal UNII lookup
ZXE7LB03WCInternal UNII lookup
F1T8QT9U8BInternal UNII lookup
G59M7S0WS3Internal UNII lookup
9I4XB1GP2BInternal UNII lookup
E7M31AEM0LInternal UNII lookup
3JYG22FD73Internal UNII lookup
VSW71SS07IInternal UNII lookup
I0V66KI1LDInternal UNII lookup

Harmonized SPL set identifiers#

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

Identifier, FDA.report destination table
IdentifierFDA.report destination
72c37485-2334-4a80-b304-1096df25c62bAvailable on FDA.report

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
7480e90b-004b-ebe4-2243-4f2fefdd9e78Product name220260128
3f158398-73f2-4b90-47d1-5c60e8719a98Product name920250721
ca6149a6-ded3-9f17-6c41-3e88f2c0c9c0Product name220250117
00358076-c817-430b-b924-11d717dc307cProduct name120160718
669af5aa-14f3-3df7-f100-5f580ffd43c1Product name120140508
6ff3bab7-2dce-8bea-d7ce-54687f0c01fbProduct name120140508
8bb82a1c-d0d0-fc27-011f-172e545f0382Product name120140508
cb03406d-e223-80bb-67d8-be80f9b6a4f2Product name120140508

FDA-Initiated Inactive NDC Indexing#

Effective, Related label table
EffectiveRelated label
2026-01-09C97
2026-01-09C97
2024-01-30C97
2024-01-30C97

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
63083-2097-2Adjustment Disorders Formula209759 mL in 1 BOTTLE, DROPPERLIQUID592

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
63083-2097ADJUSTMENT DISORDERS FORMULA 2097 (ADJUSTMENT DISORDERS FORMULA) LIQUID [PROFESSIONAL COMPLEMENTARY HEALTH FORMULAS]1Current NDC, Legacy NDC, 1 package rows20220215_72c37485-2334-4a80-b304-1096df25c62b.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
Adjustment Disorders Formula 2097ADJUSTMENT DISORDERS FORMULAProfessional Complementary Health Formulas72c37485-2334-4a80-b304-1096df25c62b2026-01-08WarningsExact identifier
ndc (package): 63083-2097-2
ndc (product): 63083-2097
ndc11 (package): 63083209702

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
63083-2097-26308320970259 mL in 1 BOTTLE, DROPPER (63083-2097-2) 59 ml1985-08-150000-00-00NoNoCurrent