Spinalmax

Product NDC
43742-1326
11-digit product format
437421326
Labeler code
43742
Product ID
43742-1326_a08a46a4-cb9e-442b-8639-967163c0b1eb
Type
HUMAN OTC DRUG
Nonproprietary name
Berberis Vulgaris, Cimicifuga Racemosa, Cinchona Officinalis, Colocynthis, Ledum Palustre, Ranunculus Bulbosus, Aesculus Hippocastanum, Cuprum Aceticum, Nadidum, Natrum Oxalaceticum, Nicotinamidum, Pyridoxinum Hydrochloricum, Riboflavinum, Thiaminum Hydrochloricum, Alpha-Lipoicum Acidum, Ammonium Muriaticum, Cartilago Suis, Discus Intervertebralis (Suis), Picricum Acidum, Silicea, Argentum Metallicum, Calcarea Phosphorica, Funiculus Umbilicalis Suis, Glandula Suprarenalis Suis, Gnaphalium Polycephalum
Dosage form
LIQUID
Route
ORAL
Labeler
Deseret Biologicals, Inc.
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2019-05-17
Substance
ALPHA LIPOIC ACID; AMMONIUM CHLORIDE; BERBERIS VULGARIS ROOT BARK; BLACK COHOSH; CINCHONA OFFICINALIS BARK; CITRULLUS COLOCYNTHIS FRUIT PULP; CUPRIC ACETATE; ENTEROBACTER CLOACAE; HORSE CHESTNUT; MERCURIC OXIDE; NADIDE; NIACINAMIDE; PANTOTHENIC ACID; PICRIC ACID; PROTEUS MORGANII; PROTEUS VULGARIS; PSEUDOGNAPHALIUM OBTUSIFOLIUM WHOLE; PYRIDOXINE HYDROCHLORIDE; RANUNCULUS BULBOSUS; RHODODENDRON TOMENTOSUM LEAFY TWIG; RIBOFLAVIN; SALMONELLA ENTERICA SUBSP. ENTERICA SEROVAR ENTERITIDIS; SILICON DIOXIDE; SILVER; SODIUM DIETHYL OXALACETATE; SULFUR; SUS SCROFA ADRENAL GLAND; SUS SCROFA BONE MARROW; SUS SCROFA CARTILAGE; SUS SCROFA INTERVERTEBRAL DISC; SUS SCROFA UMBILICAL CORD; THIAMINE HYDROCHLORIDE; TRIBASIC CALCIUM PHOSPHATE
Active strength
8; 8; 4; 4; 4; 4; 6; 30; 6; 10; 6; 6; 10; 8; 30; 30; 10; 6; 4; 4; 6; 30; 8; 10; 6; 28; 10; 10; 8; 8; 10; 6; 10 [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_C]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_C]/mL; [hp_C]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_C]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL
Pharmacologic classes
Analogs/Derivatives [Chemical/Ingredient], Blood Coagulation Factor [EPC], Calcium [CS], Cations, Divalent [CS], Increased Coagulation Factor Activity [PE], Phosphate Binder [EPC], Phosphate Chelating Activity [MoA], Vitamin B 6 [Chemical/Ingredient], Vitamin B6 Analog [EPC]
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Additional Listing Data#

Finished product
Yes
Brand name base
Spinalmax
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
BERBERIS VULGARIS ROOT BARK8 [hp_X]/mL
BLACK COHOSH8 [hp_X]/mL
CINCHONA OFFICINALIS BARK4 [hp_X]/mL
CITRULLUS COLOCYNTHIS FRUIT PULP4 [hp_X]/mL
RHODODENDRON TOMENTOSUM LEAFY TWIG4 [hp_X]/mL
RANUNCULUS BULBOSUS4 [hp_X]/mL
HORSE CHESTNUT6 [hp_X]/mL
CUPRIC ACETATE30 [hp_C]/mL
NADIDE6 [hp_X]/mL
SODIUM DIETHYL OXALACETATE10 [hp_X]/mL
NIACINAMIDE6 [hp_X]/mL
PYRIDOXINE HYDROCHLORIDE6 [hp_X]/mL
RIBOFLAVIN10 [hp_X]/mL
THIAMINE HYDROCHLORIDE8 [hp_X]/mL
ALPHA LIPOIC ACID30 [hp_C]/mL
AMMONIUM CHLORIDE30 [hp_C]/mL
SUS SCROFA CARTILAGE10 [hp_X]/mL
SUS SCROFA INTERVERTEBRAL DISC6 [hp_X]/mL
PICRIC ACID4 [hp_X]/mL
SILICON DIOXIDE4 [hp_X]/mL
SILVER6 [hp_X]/mL
TRIBASIC CALCIUM PHOSPHATE30 [hp_C]/mL
SUS SCROFA UMBILICAL CORD8 [hp_X]/mL
SUS SCROFA ADRENAL GLAND10 [hp_X]/mL
PSEUDOGNAPHALIUM OBTUSIFOLIUM WHOLE6 [hp_X]/mL
SUS SCROFA BONE MARROW28 [hp_X]/mL
MERCURIC OXIDE10 [hp_X]/mL
PANTOTHENIC ACID10 [hp_X]/mL
SULFUR8 [hp_X]/mL
ENTEROBACTER CLOACAE8 [hp_X]/mL
SALMONELLA ENTERICA SUBSP. ENTERICA SEROVAR ENTERITIDIS10 [hp_X]/mL
PROTEUS MORGANII6 [hp_X]/mL
PROTEUS VULGARIS10 [hp_X]/mL

Harmonized UNII identifiers#

UNII identifiers page 1 of 2 · 33 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
1TH8Q20J0UInternal UNII lookup
K73E24S6X9Internal UNII lookup
S003A158SBInternal UNII lookup
23H32AOH17Internal UNII lookup
877L01IZ0PInternal UNII lookup
AEQ8NXJ0MBInternal UNII lookup
3C18L6RJAZInternal UNII lookup
39M11XPH03Internal UNII lookup
0U46U6E8UKInternal UNII lookup
6CA025Y4FGInternal UNII lookup
25X51I8RD4Internal UNII lookup
68Y4CF58BVInternal UNII lookup
TLM2976OFRInternal UNII lookup
M572600E5PInternal UNII lookup
73Y7P0K73YInternal UNII lookup
01Q9PC255DInternal UNII lookup
73ECW5WG2FInternal UNII lookup
OJ17O2WTSMInternal UNII lookup
A49OS0F91SInternal UNII lookup
ETJ7Z6XBU4Internal UNII lookup

Harmonized SPL set identifiers#

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

Identifier, FDA.report destination table
IdentifierFDA.report destination
6c569331-2167-44bb-ace6-13340e7d8d6aAvailable on FDA.report

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
cf050ccd-1144-f76a-e00d-e5698d8597d4Product name620250625
bee4fa8d-8d82-423a-a0b5-40a89dd13a99Product name120250618
e0d2eb29-08bd-4bba-90d1-c91c68a38767Product name420250516
30b0ac6e-02aa-0e5c-0d8b-cffdf3a282b2Product name520250304
59361619-24d9-b610-eca6-5a7f25ed5e03Product name520240909
334fe8d2-68fb-4331-a576-420e302ec069Product name720240320
0306390c-dd77-4363-afe0-63c58088b2a1Product name120220120
503ea967-4b9c-48cf-9e87-c7975295849dProduct name220220120
444b3e50-f226-46ef-bfca-2e7035d140cdProduct name120190611
e92765c1-be81-432a-b909-1b10777ec378Product name120190208
7cda52fc-125f-421c-8fea-bc1974370c49Product name220180703
5e18e798-5614-cf5c-0185-38b1cb77a093Product name220160822
d5e51f11-ad28-caa4-4b49-4143974782adProduct name120150831
0ca1d589-929b-4b33-bc5b-1d84abdafa6aProduct name120150324
fc363c46-397b-4476-ac0f-70e43e8e4592Product name120150324
0441a8f5-3835-497c-aedd-bc78cba56b2aProduct name120150317
87711080-88eb-65c5-b2dd-bf99e700a372Product name120140508
ec2149b3-5c6d-5344-f757-c86411073075Product name120140508

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
43742-1326-1Spinalmax30 mL in 1 BOTTLE, DROPPERLIQUID307

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
43742-1326SPINALMAX (BERBERIS VULGARIS, CIMICIFUGA RACEMOSA, CINCHONA OFFICINALIS, COLOCYNTHIS, LEDUM PALUSTRE, RANUNCULUS BULBOSUS, AESCULUS HIPPOCASTANUM, CUPRUM ACETICUM, NADIDUM, NATRUM OXALACETICUM, NICOTINAMIDUM, PYRIDOXINUM HYDROCHLORICUM, RIBOFLAVINUM, THIAMINUM HYDROCHLORICUM, ALPHA-LIPOICUM ACIDUM, AMMONIUM MURIATICUM, CARTILAGO SUIS, DISCUS INTERVERTEBRALIS (SUIS), PICRICUM ACIDUM, SILICEA, ARGENTUM METALLICUM, CALCAREA PHOSPHORICA, FUNICULUS UMBILICALIS SUIS, GLANDULA SUPRARENALIS SUIS, GNAPHALIUM POLYCEPHALUM) LIQUID [DESERET BIOLOGICALS, INC.]7Current NDC, Legacy NDC, 1 package rows20240312_6c569331-2167-44bb-ace6-13340e7d8d6a.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
SpinalmaxBERBERIS VULGARIS, CIMICIFUGA RACEMOSA, CINCHONA OFFICINALIS, COLOCYNTHIS, LEDUM PALUSTRE, RANUNCULUS BULBOSUS, AESCULUS HIPPOCASTANUM, CUPRUM ACETICUM, NADIDUM, NATRUM OXALACETICUM, NICOTINAMIDUM, PYRIDOXINUM HYDROCHLORICUM, RIBOFLAVINUM, THIAMINUM HYDROCHLORICUM, ALPHA-LIPOICUM ACIDUM, AMMONIUM MURIATICUM, CARTILAGO SUIS, DISCUS INTERVERTEBRALIS (SUIS), PICRICUM ACIDUM, SILICEA, ARGENTUM METALLICUM, CALCAREA PHOSPHORICA, FUNICULUS UMBILICALIS SUIS, GLANDULA SUPRARENALIS SUIS, GNAPHALIUM POLYCEPHALUMDeseret Biologicals, Inc.6c569331-2167-44bb-ace6-13340e7d8d6a2024-03-11WarningsExact identifier
ndc (product): 43742-1326

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
43742-1326-14374213260130 mL in 1 BOTTLE, DROPPER (43742-1326-1) 30 ml2019-05-170000-00-00NoNoCurrent