FDA.reportPublic FDA data

Mercurius Combination

Product NDC
63083-9233
11-digit product format
630839233
Labeler code
63083
Product ID
63083-9233_6807acea-520d-4492-b4cd-03e2d6ef8863
Type
HUMAN OTC DRUG
Nonproprietary name
Mercurius Combination
Dosage form
LIQUID
Route
ORAL
Labeler
Professional Complementary Health Formulas
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
1984-08-15
Substance
AILANTHUS ALTISSIMA FLOWERING TWIG; AMARYLLIS BELLADONNA WHOLE; ARSENIC TRIOXIDE; CALCIUM SULFIDE; DAPHNE MEZEREUM BARK; ECHINACEA ANGUSTIFOLIA WHOLE; HUMAN HERPESVIRUS 1; LACHESIS MUTA VENOM; MERCURIUS SOLUBILIS; PHYTOLACCA AMERICANA ROOT; RECOMBINANT VARICELLA ZOSTER VIRUS GLYCOPROTEIN E ANTIGEN
Active strength
3; 4; 12; 8; 9; 3; 12; 12; 12; 4; 12 [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; [hp_X]/29.5mL
NDC exclude flag
No
Listing certified through
2027-12-31
Current FDA listing
Yes

Additional Listing Data#

Finished product
Yes
Brand name base
Mercurius Combination
Brand name suffix
9233
Listing expiration
2027-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
AILANTHUS ALTISSIMA FLOWERING TWIG3 [hp_X]/29.5mL
AMARYLLIS BELLADONNA WHOLE4 [hp_X]/29.5mL
ARSENIC TRIOXIDE12 [hp_X]/29.5mL
CALCIUM SULFIDE8 [hp_X]/29.5mL
DAPHNE MEZEREUM BARK9 [hp_X]/29.5mL
ECHINACEA ANGUSTIFOLIA WHOLE3 [hp_X]/29.5mL
HUMAN HERPESVIRUS 112 [hp_X]/29.5mL
LACHESIS MUTA VENOM12 [hp_X]/29.5mL
MERCURIUS SOLUBILIS12 [hp_X]/29.5mL
PHYTOLACCA AMERICANA ROOT4 [hp_X]/29.5mL
RECOMBINANT VARICELLA ZOSTER VIRUS GLYCOPROTEIN E ANTIGEN12 [hp_X]/29.5mL

Harmonized Identifiers#

Field, Values table
FieldValues
Unii8P29O5P7XU, 11B89M58UN, S7V92P67HO, 1MBW07J51Q, X2N6E405GV, VB06AV5US8, 22G38P19RL, VSW71SS07I, 324Y4038G2, 11E6VI8VEG, COB9FF6I46

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
63f39a63-5cd1-4016-bd86-2bbb0f6c3139Product name320240506
e5a77e9c-c528-733a-173d-914a234c024bProduct name520240506

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
63083-9233-12026-01-07C16284748780-11030e365-6df9-111a-e063-dadaa90a10e2R233
63083-9233-12024-01-30C16284748780-11030e365-6df9-111a-e063-dadaa90a10e2R233

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
63083-9233-1Mercurius Combination923329.5 mL in 1 BOTTLE, DROPPERLIQUID29.52

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
63083-9233MERCURIUS COMBINATION 9233 (MERCURIUS COMBINATION) LIQUID [PROFESSIONAL COMPLEMENTARY HEALTH FORMULAS]1Current NDC, Legacy NDC, 1 package rows20220210_42e1d05d-c0ab-48f3-94d2-1a1d3e1d2944.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
63083-9233-16308392330129.5 mL in 1 BOTTLE, DROPPER (63083-9233-1) 29.5 ml1985-08-150000-00-00NoNoCurrent