Home NDC 57955-2817-2 Skin Irritations and Itch Relief
Product NDC 57955-2817
Requested package NDC 57955-2817-2
11-digit product format 579552817
Labeler code 57955
Product ID 57955-2817_717db916-0a68-4917-a4bc-7ea5bf48278e
Type HUMAN OTC DRUG
Nonproprietary name Agaricus muscarius, Alumina, Anagallis arvensis, Antimonium tartaricum, Apis mellifica, Arsenicum album, Arsenicum iodatum, Bovista, Causticum, Dolichos pruriens, Fagopyrum esculentum, Graphites, Kali muriaticum, Muriaticum acidum, Oleander, Petroleum, Pix liquida, Radium bromatum, Rhus toxicodendron, Selenium metallicum, Sulphur, Urtica urens.
Dosage form LIQUID
Route ORAL
Labeler King Bio Inc.
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 2022-12-07
Marketing end 0000-00-00
Substance ALUMINUM OXIDE; AMANITA MUSCARIA FRUITING BODY; ANTIMONY POTASSIUM TARTRATE; APIS MELLIFERA; ARSENIC TRIIODIDE; ARSENIC TRIOXIDE; CAUSTICUM; FAGOPYRUM ESCULENTUM WHOLE; GRAPHITE; HYDROCHLORIC ACID; KEROSENE; LYCOPERDON UTRIFORME FRUITING BODY; LYSIMACHIA ARVENSIS WHOLE; MUCUNA PRURIENS FRUIT TRICHOME; NERIUM OLEANDER LEAF; PINE TAR; POTASSIUM CHLORIDE; RADIUM BROMIDE; SELENIUM; SULFUR; TOXICODENDRON PUBESCENS LEAF; URTICA URENS WHOLE
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; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL
Pharmacologic classes Allergens [CS], Bee Venoms [CS], Cell-mediated Immunity [PE], Increased Histamine Release [PE], Increased IgG Production [PE], Increased Large Intestinal Motility [PE], Inhibition Large Intestine Fluid/Electrolyte Absorption [PE], Osmotic Activity [MoA], Osmotic Laxative [EPC], Potassium Compounds [CS], Potassium Salt [EPC], Standardized Insect Venom Allergenic Extract [EPC]
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 · 2 matching rows.
View current auxiliary records. · View the auxiliary file history.
Captured / source date, Dataset, Scope table Captured / source date Dataset Scope Product NDC Package NDC Code Status Reporting period Archive Snapshot Source SHA-256 2025-12-14 17:58 UTC · source 2025-12-05 excluded package package 57955-2817 57955-2817-2 D Discontinued by firm excluded / ndc_excluded.zip d630ba8d3edf…732f749b63fb…2025-08-27 00:01 UTC · source 2025-08-26 excluded package package 57955-2817 57955-2817-2 D Discontinued by firm excluded / ndc_excluded.zip f5e01cc5f278…a2eaf40c39c3…
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Marketing start Marketing end Sample Exclude flag Status 57955-2817-2 57955281702 1 BOTTLE, SPRAY in 1 CARTON (57955-2817-2) > 59 mL in 1 BOTTLE, SPRAY 2022-12-07 0000-00-00 No No Current