Spinalmax

Product NDC
43742-0679
11-digit product format
437420679
Labeler code
43742
Product ID
43742-0679_470e9846-d192-4e1f-a7df-34ef659af623
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, Picricum Acidum, Pyridoxinum Hydrochloricum, Riboflavinum, Thiaminum Hydrochloricum, Alpha-Lipoicum Acidum, Ammonium Muriaticum, Cartilago Suis, Discus Intervertebralis (Suis), Silicea, Argentum Metallicum, Calcarea Phosphorica, Coenzyme A, Funiculus Umbilicalis Suis, Glandula Suprarenalis Suis
Dosage form
LIQUID
Route
ORAL
Labeler
Deseret Biologicals, Inc.
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2015-12-04
Marketing end
2020-12-30
Substance
BERBERIS VULGARIS ROOT BARK; BLACK COHOSH; CINCHONA OFFICINALIS BARK; CITRULLUS COLOCYNTHIS FRUIT PULP; LEDUM PALUSTRE TWIG; RANUNCULUS BULBOSUS; HORSE CHESTNUT; CUPRIC ACETATE; NADIDE; SODIUM DIETHYL OXALACETATE; NIACINAMIDE; PICRIC ACID; PYRIDOXINE HYDROCHLORIDE; RIBOFLAVIN; THIAMINE HYDROCHLORIDE; .ALPHA.-LIPOIC ACID; AMMONIUM CHLORIDE; SUS SCROFA CARTILAGE; SUS SCROFA INTERVERTEBRAL DISC; SILICON DIOXIDE; SILVER; TRIBASIC CALCIUM PHOSPHATE; COENZYME A; SUS SCROFA UMBILICAL CORD; SUS SCROFA ADRENAL GLAND; PSEUDOGNAPHALIUM OBTUSIFOLIUM; SUS SCROFA BONE MARROW; MERCURIC OXIDE; SULFUR; ENTEROBACTER CLOACAE; SALMONELLA ENTERICA SUBSP. ENTERICA SEROVAR ENTERITIDIS; PROTEUS MORGANII; PROTEUS VULGARIS
Active strength
4 [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; [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; [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_C]/mL; [hp_C]/mL; [hp_C]/mL
NDC exclude flag
No
Listing certified through
0000-00-00
Current FDA listing
Historical FDA.report record