Vermex

Product NDC
63083-6016
11-digit product format
630836016
Labeler code
63083
Product ID
63083-6016_0f7e7e8d-f943-4f2a-b819-34143c4c775c
Type
HUMAN OTC DRUG
Nonproprietary name
Vermex
Dosage form
LIQUID
Route
ORAL
Labeler
Professional Complementary Health Formulas
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
1984-08-15
Substance
ARTEMISIA CINA PRE-FLOWERING TOP; BERBERIS VULGARIS ROOT BARK; BLACK WALNUT; CLOVE; COPPER; DRYOPTERIS FILIX-MAS ROOT; SCHOENOCAULON OFFICINALE SEED; SPIGELIA MARILANDICA ROOT; TEUCRIUM MARUM WHOLE; WORMWOOD
Active strength
2; 3; 2; 12; 6; 4; 4; 3; 3; 6 [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
Allergens [CS], Allergens [CS], Cell-mediated Immunity [PE], Cell-mediated Immunity [PE], Copper [CS], Copper-containing Intrauterine Device [EPC], Decreased Embryonic Implantation [PE], Decreased Sperm Motility [PE], Dietary Proteins [CS], Dietary Proteins [CS], Food Additives [CS], Increased Histamine Release [PE], Increased Histamine Release [PE], Inhibit Ovum Fertilization [PE], Non-Standardized Food Allergenic Extract [EPC], Non-Standardized Food Allergenic Extract [EPC], Non-Standardized Plant Allergenic Extract [EPC], Nut Proteins [EXT], 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
Vermex
Brand name suffix
6016
Listing expiration
2027-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
ARTEMISIA CINA PRE-FLOWERING TOP2 [hp_X]/59mL
BERBERIS VULGARIS ROOT BARK3 [hp_X]/59mL
BLACK WALNUT2 [hp_X]/59mL
CLOVE12 [hp_X]/59mL
COPPER6 [hp_X]/59mL
DRYOPTERIS FILIX-MAS ROOT4 [hp_X]/59mL
SCHOENOCAULON OFFICINALE SEED4 [hp_X]/59mL
SPIGELIA MARILANDICA ROOT3 [hp_X]/59mL
TEUCRIUM MARUM WHOLE3 [hp_X]/59mL
WORMWOOD6 [hp_X]/59mL

Harmonized Identifiers#

Field, Values table
FieldValues
Unii28M1820ACT, 1TH8Q20J0U, 02WM57RXZJ, K48IKT5321, 789U1901C5, C0ZK0RRF5X, 6NAF1689IO, 467D26HS0B, 10464S0TAA, F84709P2XV

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
c599c4a0-705d-4ebb-ab1f-977af038f96aProduct name120251124

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
63083-6016-22026-01-08C16284748780-11030e365-3676-111a-e063-dadaa90a10e2X16
63083-6016-22026-01-08C16284748780-11030e365-3676-111a-e063-dadaa90a10e2X16
63083-6016-22024-01-30C16284748780-11030e365-3676-111a-e063-dadaa90a10e2X16
63083-6016-22024-01-30C16284748780-11030e365-3676-111a-e063-dadaa90a10e2X16

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
63083-6016-2Vermex601659 mL in 1 BOTTLE, DROPPERLIQUID592

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
63083-6016VERMEX 6016 (VERMEX) LIQUID [PROFESSIONAL COMPLEMENTARY HEALTH FORMULAS]1Current NDC, Legacy NDC, 1 package rows20220406_a8a70546-ae5d-4524-b6bc-3dc0a989faec.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
63083-6016-26308360160259 mL in 1 BOTTLE, DROPPER (63083-6016-2) 59 ml1985-08-150000-00-00NoNoCurrent