Home NDC 57955-2822 Back, Muscle and Joint Relief
Product NDC 57955-2822
11-digit product format 579552822
Labeler code 57955
Product ID 57955-2822_5323fafe-1c8e-40d3-93bd-0558b3c7c712
Type HUMAN OTC DRUG
Nonproprietary name Aesculus hippocastanum, Arnica montana, Bellis perennis, Bryonia, Calcarea carbonica, Calcarea fluorica, Cimicifuga racemosa, Cobaltum metallicum, Gnaphalium polycephalum, Hypericum perforatum, Kali carbonicum, Kali phosphoricum, Magnesia phosphorica,Oxalicum acidum, Phosphorus, Rhus tox, Ruta graveolens, Zincum metallicum
Dosage form LIQUID
Route ORAL
Labeler King Bio Inc.
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 2022-08-25
Marketing end 0000-00-00
Substance ARNICA MONTANA WHOLE; BELLIS PERENNIS WHOLE; BLACK COHOSH; BRYONIA ALBA ROOT; CALCIUM FLUORIDE; COBALT; DIBASIC POTASSIUM PHOSPHATE; HORSE CHESTNUT; HYPERICUM PERFORATUM WHOLE; MAGNESIUM PHOSPHATE, DIBASIC TRIHYDRATE; OXALIC ACID DIHYDRATE; OYSTER SHELL CALCIUM CARBONATE, CRUDE; PHOSPHORUS; POTASSIUM CARBONATE; PSEUDOGNAPHALIUM OBTUSIFOLIUM WHOLE; RUTA GRAVEOLENS FLOWERING TOP; TOXICODENDRON PUBESCENS LEAF; ZINC
Active strength 10 [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL
Pharmacologic classes Allergens [CS], Calculi Dissolution Agent [EPC], Cell-mediated Immunity [PE], Increased Histamine Release [PE], Increased Large Intestinal Motility [PE], Inhibition Large Intestine Fluid/Electrolyte Absorption [PE], Inhibition Small Intestine Fluid/Electrolyte Absorption [PE], Magnesium Ion Exchange Activity [MoA], Osmotic Activity [MoA], Osmotic Laxative [EPC], Standardized Chemical Allergen [EPC], Stimulation Large Intestine Fluid/Electrolyte Secretion [PE]
NDC exclude flag No
Listing certified through 2023-12-31
Current FDA listing Historical FDA.report record Observed NDC auxiliary status history# This history shows the information present in each captured FDA auxiliary file. It is not a continuous regulatory timeline, and a missing record does not establish a status.
Historic NDC status page 1 of 1 · 4 matching rows.
View current auxiliary records. · View the auxiliary file history.
Captured / source date, Dataset, Scope table Captured / source date Dataset Scope Package NDC Snapshot Source SHA-256 2025-12-14 17:58 UTC · source 2025-12-05 excluded product product d630ba8d3edf…732f749b63fb…2025-12-14 17:58 UTC · source 2025-12-05 excluded package package 57955-2822-2 d630ba8d3edf…732f749b63fb…2025-08-27 00:01 UTC · source 2025-08-26 excluded product product f5e01cc5f278…a2eaf40c39c3…2025-08-27 00:01 UTC · source 2025-08-26 excluded package package 57955-2822-2 f5e01cc5f278…a2eaf40c39c3…
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 57955-2822 BACK, MUSCLE AND JOINT RELIEF (AESCULUS HIPPOCASTANUM, ARNICA MONTANA, BELLIS PERENNIS, BRYONIA, CALCAREA CARBONICA, CALCAREA FLUORICA, CIMICIFUGA RACEMOSA, COBALTUM METALLICUM, GNAPHALIUM POLYCEPHALUM, HYPERICUM PERFORATUM, KALI CARBONICUM, KALI PHOSPHORICUM, MAGNESIA PHOSPHORICA,OXALICUM ACIDUM, PHOSPHORUS, RHUS TOX, RUTA GRAVEOLENS, ZINCUM METALLICUM) LIQUID [KING BIO INC.] 3 Legacy NDC 20250522_b4c23381-8bca-4159-98d5-557e188c14af.zip
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Marketing start Marketing end Sample Exclude flag Status 57955-2822-2 57955282202 1 BOTTLE, SPRAY in 1 CARTON (57955-2822-2) > 59 mL in 1 BOTTLE, SPRAY 2022-08-25 0000-00-00 No No Current