Spinalmax
- Product NDC
- 43742-0757
- 11-digit product format
- 437420757
- Labeler code
- 43742
- Product ID
- 43742-0757_7bc598f5-c8ef-4344-9ea8-4790868dde2f
- 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, Funiculus Umbilicalis Suis, Glandula Suprarenalis Suis, Gnaphalium Polycephalum
- Dosage form
- LIQUID
- Route
- ORAL
- Labeler
- Deseret Biologicals, Inc.
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2016-05-31
- Marketing end
- 2023-08-16
- 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; THIOCTIC ACID; AMMONIUM CHLORIDE; SUS SCROFA CARTILAGE; SUS SCROFA INTERVERTEBRAL DISC; SILICON DIOXIDE; SILVER; TRIBASIC CALCIUM PHOSPHATE; SUS SCROFA UMBILICAL CORD; SUS SCROFA ADRENAL GLAND; PSEUDOGNAPHALIUM OBTUSIFOLIUM; SUS SCROFA BONE MARROW; MERCURIC OXIDE; PANTOTHENIC ACID; 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
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 43742-0757-1 | 43742075701 | 30 mL in 1 BOTTLE, DROPPER (43742-0757-1) | 30 ml | 2017-03-30 | 2023-08-16 | No | No | Current |