Over-the-counter drug · UNAPPROVED HOMEOPATHIC
Spinalmax NDC 43742-1326
Berberis vulgaris root bark 4 [hp_X]/mL + 32 more ingredients · Liquid · Oral · Deseret Biologicals, Inc.
NDC codes
FDA NDC Directory| Package NDC | 11-digit (billing) | Package | Copy |
|---|---|---|---|
| 43742-1326-1 | 43742132601 | 30 mL in 1 BOTTLE, DROPPER (43742-1326-1)Marketed from May 17, 2019 |
How the 11-digit form is made: The package segment has 1 digit, so one leading zero is added to it (5-4-1 → 5-4-2). Formatting the NDC does not by itself make it billable — the product, package and quantity must match what was dispensed or administered, and payer rules apply. Conversion rules
Product information
- Brand name (proprietary)
- Spinalmax
- Generic name (nonproprietary)
- 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
- Active ingredients
- Berberis vulgaris root bark — 4 [hp_X]/mLBlack cohosh — 4 [hp_X]/mLCinchona officinalis bark — 4 [hp_X]/mLCitrullus colocynthis fruit pulp — 4 [hp_X]/mLRhododendron tomentosum leafy twig — 4 [hp_X]/mLRanunculus bulbosus — 4 [hp_X]/mLHorse chestnut — 6 [hp_X]/mLCupric acetate — 6 [hp_X]/mLNadide — 6 [hp_X]/mLSodium diethyl oxalacetate — 6 [hp_X]/mLNiacinamide — 6 [hp_X]/mLPyridoxine hydrochloride — 6 [hp_X]/mLRiboflavin — 6 [hp_X]/mLThiamine hydrochloride — 6 [hp_X]/mLAlpha lipoic acid — 8 [hp_X]/mLAmmonium chloride — 8 [hp_X]/mLSus scrofa cartilage — 8 [hp_X]/mLSus scrofa intervertebral disc — 8 [hp_X]/mLPicric acid — 8 [hp_X]/mLSilicon dioxide — 8 [hp_X]/mLSilver — 10 [hp_X]/mLTribasic calcium phosphate — 10 [hp_X]/mLSus scrofa umbilical cord — 10 [hp_X]/mLSus scrofa adrenal gland — 10 [hp_X]/mLPseudognaphalium obtusifolium whole — 10 [hp_X]/mLSus scrofa bone marrow — 10 [hp_X]/mLMercuric oxide — 10 [hp_X]/mLPantothenic acid — 10 [hp_X]/mLSulfur — 28 [hp_X]/mLEnterobacter cloacae — 30 [hp_C]/mLSalmonella enterica subsp. Enterica serovar enteritidis — 30 [hp_C]/mLProteus morganii — 30 [hp_C]/mLProteus vulgaris — 30 [hp_C]/mL
- Dosage form
- Liquid
- Route
- Oral
- Labeler
- Deseret Biologicals, Inc.
- Product type
- Over-the-counter drug
- Marketing category
- Unapproved homeopathic
- Marketing start
- Listing expires
- Other FDA classes
- Analogs/Derivatives (Chemical/Ingredient)Calcium (Chemical structure)Divalent (Chemical structure)Increased Coagulation Factor Activity (Physiologic effect)Phosphate Chelating Activity (Mechanism)Vitamin B 6 (Chemical/Ingredient)
- Identifiers
- Product ID 43742-1326_a08a46a4-cb9e-442b-8639-967163c0b1ebSPL ID a08a46a4-cb9e-442b-8639-967163c0b1ebSPL set ID 6c569331-2167-44bb-ace6-13340e7d8d6aUNII 1TH8Q20J0U, K73E24S6X9, S003A158SB, 23H32AOH17, 877L01IZ0P, AEQ8NXJ0MB, 3C18L6RJAZ, 39M11XPH03, 0U46U6E8UK, 6CA025Y4FG, 25X51I8RD4, 68Y4CF58BV, TLM2976OFR, M572600E5P, 73Y7P0K73Y, 01Q9PC255D, 73ECW5WG2F, OJ17O2WTSM, A49OS0F91S, ETJ7Z6XBU4, 3M4G523W1G, 91D9GV0Z28, 118OYG6W3H, 398IYQ16YV, 36XQ854NWW, VP2CN2G7Y8, IY191986AO, 19F5HK2737, 70FD1KFU70, 40OMQ8YEPD, Y3V16D4PV4, 56X6LID5ZY, 11T9HCO30OUPC 0810151880815
- Pharmacologic class
- Blood Coagulation Factor; Phosphate Binder; Vitamin B6 Analog
Billing references
What Med-Code can say about coding this product, and where each statement comes from. Nothing here is inferred from the name alone.
- HCPCS codeNo match
No HCPCS code in Med-Code's directory. Oral products like this are usually dispensed by a pharmacy and billed by NDC.
- NDC on a medical claim
N443742132601followed by a unit qualifier and the quantityPackage 43742-1326-01. Unit qualifiers: F2 (international unit), GR (gram), ME (milligram), ML (milliliter), UN (unit (each)). The qualifier and quantity depend on what was given. About the N4 qualifier
Product label
Current FDA label (SPL), effective .
Indications (excerpt from the label)
INDICATION: • For the temporary relief of symptoms including: • back discomfort • back spasms • back pain • anxiety • nervousness These statements are based upon homeopathic principles. They have not been reviewed by the Food and Drug Administration.
Excerpt only. Read the full label for complete information.