FDA.reportPublic FDA data

Secale Combination

Product NDC
63083-9244
11-digit product format
630839244
Labeler code
63083
Product ID
63083-9244_67d19e12-8277-4790-a3bf-0979a9c7dc8c
Type
HUMAN OTC DRUG
Nonproprietary name
Secale Combination
Dosage form
LIQUID
Route
ORAL
Labeler
Professional Complementary Health Formulas
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
1984-08-15
Substance
ARNICA MONTANA WHOLE; ARSENIC TRIOXIDE; AVISCUMINE; BARIUM IODIDE; CLAVICEPS PURPUREA SCLEROTIUM; OYSTER SHELL CALCIUM CARBONATE, CRUDE; PHOSPHORUS; SILVER NITRATE; SOLANUM NIGRUM TOP; TOBACCO LEAF
Active strength
12; 12; 4; 6; 4; 4; 8; 6; 4; 8 [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; [hp_X]/29.5mL
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]
NDC exclude flag
No
Listing certified through
2027-12-31
Current FDA listing
Yes

Additional Listing Data#

Finished product
Yes
Brand name base
Secale Combination
Brand name suffix
9244
Listing expiration
2027-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
ARNICA MONTANA WHOLE12 [hp_X]/29.5mL
ARSENIC TRIOXIDE12 [hp_X]/29.5mL
AVISCUMINE4 [hp_X]/29.5mL
BARIUM IODIDE6 [hp_X]/29.5mL
CLAVICEPS PURPUREA SCLEROTIUM4 [hp_X]/29.5mL
OYSTER SHELL CALCIUM CARBONATE, CRUDE4 [hp_X]/29.5mL
PHOSPHORUS8 [hp_X]/29.5mL
SILVER NITRATE6 [hp_X]/29.5mL
SOLANUM NIGRUM TOP4 [hp_X]/29.5mL
TOBACCO LEAF8 [hp_X]/29.5mL

Harmonized Identifiers#

Field, Values table
FieldValues
UniiO80TY208ZW, S7V92P67HO, 4B18YVW82N, WKC4T7680A, 01G9XEA93N, 2E32821G6I, 27YLU75U4W, 95IT3W8JZE, O4G5C1G3W5, 6YR2608RSU

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
63f39a63-5cd1-4016-bd86-2bbb0f6c3139Product name320240506
e5a77e9c-c528-733a-173d-914a234c024bProduct name520240506
6cca4355-1206-91f7-02de-17eef38a8622Product name120140508
751c581a-bf64-2fd7-b3ec-ca02c83e4a00Product name120140508

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
63083-9244-12026-01-09C16284748780-11030e365-4928-111a-e063-dadaa90a10e2R244
63083-9244-12026-01-09C16284748780-11030e365-4928-111a-e063-dadaa90a10e2R244
63083-9244-12024-01-30C16284748780-11030e365-4928-111a-e063-dadaa90a10e2R244
63083-9244-12024-01-30C16284748780-11030e365-4928-111a-e063-dadaa90a10e2R244

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
63083-9244-1Secale Combination924429.5 mL in 1 BOTTLE, DROPPERLIQUID29.52

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
63083-9244SECALE COMBINATION 9244 (SECALE COMBINATION) LIQUID [PROFESSIONAL COMPLEMENTARY HEALTH FORMULAS]1Current NDC, Legacy NDC, 1 package rows20220210_6f68121f-48ac-478c-ad02-434db259920a.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
63083-9244-16308392440129.5 mL in 1 BOTTLE, DROPPER (63083-9244-1) 29.5 ml1985-08-150000-00-00NoNoCurrent