Arthritis Joints
- Product NDC
- 43742-0133
- 11-digit product format
- 437420133
- Labeler code
- 43742
- Product ID
- 43742-0133_ed53a297-1327-4569-9fd4-981a9161ea00
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Gnaphalium Polycephalum, Berberis Vulgaris, Cimicifuga Racemosa, Cinchona Officinalis, Colocynthis, Ledum Palustre, Ranunculus Bulbosus, Aesculus Hippocastanum, Borax, Cuprum Aceticum, Kali Carbonicum, Pulsatilla, Secale Cornutum, Ammonium Muriaticum, Silicea, Argentum Metallicum, Calcarea Phosphorica, Glandula Suprarenalis Suis, Mercurius Praecipitatus Ruber, Sepia, Zincum Metallicum, Palladium Metallicum, Picricum Acidum, Sulphur, Cartilago Suis, Intervertebral Disc (Suis), Medulla Ossis Suis
- Dosage form
- LIQUID
- Route
- ORAL
- Labeler
- Deseret Biologicals, Inc.
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2012-09-12
- Marketing end
- 2020-09-08
- Substance
- PSEUDOGNAPHALIUM OBTUSIFOLIUM; BERBERIS VULGARIS ROOT BARK; BLACK COHOSH; CINCHONA OFFICINALIS BARK; CITRULLUS COLOCYNTHIS FRUIT PULP; LEDUM PALUSTRE TWIG; RANUNCULUS BULBOSUS; HORSE CHESTNUT; SODIUM BORATE; CUPRIC ACETATE; POTASSIUM CARBONATE; PULSATILLA VULGARIS; CLAVICEPS PURPUREA SCLEROTIUM; AMMONIUM CHLORIDE; SILICON DIOXIDE; SILVER; TRIBASIC CALCIUM PHOSPHATE; SUS SCROFA ADRENAL GLAND; MERCURIC OXIDE; SEPIA OFFICINALIS JUICE; ZINC; PALLADIUM; PICRIC ACID; SULFUR; SUS SCROFA CARTILAGE; SUS SCROFA INTERVERTEBRAL DISC; SUS SCROFA BONE MARROW
- Active strength
- 3 [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; 1/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