Skin Irritations and Itch Relief
- Product NDC
- 57955-2817
- 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
NDC auxiliary status#
These records are reproduced from FDA’s unfinished, excluded, and compounder listings. They describe what appeared in the source files; a missing record does not establish a regulatory status. View all current auxiliary records, including entries without an NDC. · View the auxiliary file history.
| Dataset | Scope | Product NDC | Package NDC | Code | Status | Reporting period | Source date |
|---|---|---|---|---|---|---|---|
| excluded product | product | 57955-2817 | D | Discontinued by firm | 2026-09-14 | ||
| excluded package | package | 57955-2817 | 57955-2817-2 | D | Discontinued by firm | 2026-09-14 |
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.
| 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 | 57955-2817-2 | 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 | 57955-2817-2 | f5e01cc5f278… | a2eaf40c39c3… |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.
Packages#
| 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 |