FDA.reportPublic FDA data

VertiFix

Product NDC
70163-0008
11-digit product format
701630008
Labeler code
70163
Product ID
70163-0008_2e71d9a7-f63a-4c40-84e6-f7cf248d61f1
Type
HUMAN OTC DRUG
Nonproprietary name
Argentum Nitricum, Bryonia (Alba), Causticum, Cocculus Indicus, Gelsemium Sempervirens, Ipecacuanha, Nux Vomica, Petroleum, Sulphur, Tabacum
Dosage form
TABLET
Route
ORAL
Labeler
NaturalCare
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2026-03-11
Substance
ANAMIRTA COCCULUS SEED; BRYONIA ALBA ROOT; CAUSTICUM; GELSEMIUM SEMPERVIRENS ROOT; IPECAC; KEROSENE; SILVER NITRATE; STRYCHNOS NUX-VOMICA SEED; SULFUR; TOBACCO LEAF
Active strength
6; 30; 12; 12; 6; 12; 30; 6; 12; 6 [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1
Pharmacologic classes
Allergens [CS], Allergens [CS], Cell-mediated Immunity [PE], Cell-mediated Immunity [PE], Increased Histamine Release [PE], Increased Histamine Release [PE], Increased IgG Production [PE], Increased IgG Production [PE], Non-Standardized Plant Allergenic Extract [EPC], Non-Standardized Plant Allergenic Extract [EPC], Plant Proteins [CS], Plant Proteins [CS], Seed Storage 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
VertiFix
Listing expiration
2027-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
SILVER NITRATE6 [hp_X]/1
BRYONIA ALBA ROOT30 [hp_X]/1
CAUSTICUM12 [hp_X]/1
ANAMIRTA COCCULUS SEED12 [hp_X]/1
GELSEMIUM SEMPERVIRENS ROOT6 [hp_X]/1
IPECAC12 [hp_X]/1
STRYCHNOS NUX-VOMICA SEED30 [hp_X]/1
KEROSENE6 [hp_X]/1
SULFUR12 [hp_X]/1
TOBACCO LEAF6 [hp_X]/1

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 10 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
95IT3W8JZEInternal UNII lookup
T7J046YI2BInternal UNII lookup
DD5FO1WKFUInternal UNII lookup
810258W28UInternal UNII lookup
639KR60Q1QInternal UNII lookup
62I3C8233LInternal UNII lookup
269XH13919Internal UNII lookup
1C89KKC04EInternal UNII lookup
70FD1KFU70Internal UNII lookup
6YR2608RSUInternal UNII lookup

Harmonized SPL set identifiers#

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

Identifier, FDA.report destination table
IdentifierFDA.report destination
33b00f06-3202-4904-855c-cdfaa93677a4Available on FDA.report

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
6cca4355-1206-91f7-02de-17eef38a8622Product name120140508
751c581a-bf64-2fd7-b3ec-ca02c83e4a00Product name120140508

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
70163-0008-1VertiFix60 in 1 BLISTER PACKTABLET601
70163-0008-1VertiFix1 in 1 CARTONTABLET11

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
VertiFixARGENTUM NITRICUM, BRYONIA (ALBA), CAUSTICUM, COCCULUS INDICUS, GELSEMIUM SEMPERVIRENS, IPECACUANHA, NUX VOMICA, PETROLEUM, SULPHUR, TABACUMNaturalCare33b00f06-3202-4904-855c-cdfaa93677a42026-03-11WarningsExact identifier
ndc (product): 70163-0008

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
70163-0008-1701630008011 BLISTER PACK in 1 CARTON (70163-0008-1) / 60 TABLET in 1 BLISTER PACK1 blister pack2026-03-11NoNoCurrent