What is NDC 57955-9968?

57955-9968 is the product NDC for Skin Irritations and Itch Relief, Amanita muscaria fruiting body 10 [hp_X]/59mL + 21 more ingredients liquid, listed with the FDA by King Bio Inc.. It has 1 package NDC, shown above in 10- and 11-digit form.

What drug is associated with this NDC?

Skin Irritations and Itch Relief (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 (12X, 30X, 1LM), Rhus tox, Selenium metallicum, Sulphur and Urtica urens.).

What is the active ingredient?

Amanita muscaria fruiting body, Aluminum oxide, Lysimachia arvensis whole, Antimony potassium tartrate, Apis mellifera, Arsenic trioxide, Arsenic triiodide, Lycoperdon utriforme fruiting body, Causticum, Mucuna pruriens fruit trichome, Fagopyrum esculentum whole, Graphite, Potassium chloride, Hydrochloric acid, Nerium oleander leaf, Liquid petroleum, Pine tar, Radium bromide, Toxicodendron pubescens leaf, Selenium, Sulfur, Urtica urens whole.

King Bio Inc., NDC labeler code 57955. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.

What other NDCs exist for Skin Irritations and Itch Relief?

None: this is the only finished product listed under this name.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

Skin Irritations and Itch Relief NDC 57955-9968

NDC codes

FDA NDC Directory

Product NDC (as listed)57955-9968Labeler and product segments. Claims need a package NDC.

Product NDC at billing width57955-9968Add the package segment from the table below.

Package NDCs as listed with the FDA, and the 11-digit 5-4-2 form used on claims. The highlighted digit is the added leading zero.
Package NDC	11-digit (billing)	Package	Copy
57955-9968-2	5795599680257955996802	59 mL in 1 BOTTLE, SPRAY (57955-9968-2)Marketed from Mar 13, 2026

How the 11-digit form is made: The package segment has 1 digit, so one leading zero is added to it (5-4-1 → 5-4-2). Formatting the NDC does not by itself make it billable — the product, package and quantity must match what was dispensed or administered, and payer rules apply. Conversion rules

Product information

Brand name (proprietary): Skin Irritations and Itch Relief
Generic name (nonproprietary): 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 (12x, 30x, 1lm), rhus tox, selenium metallicum, sulphur and urtica urens.
Active ingredients: Amanita muscaria fruiting body — 10 [hp_X]/59mLAluminum oxide — 10 [hp_X]/59mLLysimachia arvensis whole — 10 [hp_X]/59mLAntimony potassium tartrate — 10 [hp_X]/59mLApis mellifera — 10 [hp_X]/59mLArsenic trioxide — 10 [hp_X]/59mLArsenic triiodide — 10 [hp_X]/59mLLycoperdon utriforme fruiting body — 10 [hp_X]/59mLCausticum — 10 [hp_X]/59mLMucuna pruriens fruit trichome — 10 [hp_X]/59mLFagopyrum esculentum whole — 10 [hp_X]/59mLGraphite — 10 [hp_X]/59mLPotassium chloride — 10 [hp_X]/59mLHydrochloric acid — 10 [hp_X]/59mLNerium oleander leaf — 10 [hp_X]/59mLLiquid petroleum — 10 [hp_X]/59mLPine tar — 10 [hp_X]/59mLRadium bromide — 12 [hp_X]/59mLToxicodendron pubescens leaf — 10 [hp_X]/59mLSelenium — 10 [hp_X]/59mLSulfur — 10 [hp_X]/59mLUrtica urens whole — 10 [hp_X]/59mL
Dosage form: Liquid
Route: Oral
Labeler: King Bio Inc.NDC labeler code 57955
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Mar 13, 2026
Listing expires: Dec 31, 2027
Other FDA classes: Allergens (Chemical structure)Bee Venoms (Chemical structure)Cell-mediated Immunity (Physiologic effect)Increased Histamine Release (Physiologic effect)Increased IgG Production (Physiologic effect)Increased Large Intestinal Motility (Physiologic effect)Inhibition Large Intestine Fluid/Electrolyte Absorption (Physiologic effect)Osmotic Activity (Mechanism)Potassium Compounds (Chemical structure)
Identifiers: Product ID 57955-9968_01a197b3-f8c2-4df5-8655-3cff6972249eSPL ID 01a197b3-f8c2-4df5-8655-3cff6972249eSPL set ID d139d2f1-0369-4963-9f3d-c4cc0f1ea2ddUNII DIF093I037, LMI26O6933, 46883LR90E, DL6OZ476V3, 7S82P3R43Z, S7V92P67HO, 3029988O2T, K2A74U428F, DD5FO1WKFU, 3E271BSI0C, B10M69172N, 4QQN74LH4O, 660YQ98I10, QTT17582CB, 7KV510R6H6, 6ZAE7X688J, YFH4WC535J, R74O7T8569, 6IO182RP7A, H6241UJ22B, 70FD1KFU70, IHN2NQ5OF9
Pharmacologic class: Osmotic Laxative; Potassium Salt; Standardized Insect Venom Allergenic Extract

Billing references

What Med-Code can say about coding this product, and where each statement comes from. Nothing here is inferred from the name alone.

HCPCS codeNo match

No HCPCS code in Med-Code's directory. Oral products like this are usually dispensed by a pharmacy and billed by NDC.

NDC on a medical claim

N457955996802 followed by a unit qualifier and the quantity

Package 57955-9968-02. Unit qualifiers: F2 (international unit), GR (gram), ME (milligram), ML (milliliter), UN (unit (each)). The qualifier and quantity depend on what was given. About the N4 qualifier

Product label

Current FDA label (SPL), effective Mar 10, 2026.

Indications (excerpt from the label)

Uses † For temporarily relief of: itching rash hives redness burning sensitivity dryness scales roughness † Claims based on traditional Homeopathic practice, not accepted medical evidence, not FDA evaluated.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 57955-9968

What is NDC 57955-9968?: 57955-9968 is the product NDC for Skin Irritations and Itch Relief, Amanita muscaria fruiting body 10 [hp_X]/59mL + 21 more ingredients liquid, listed with the FDA by King Bio Inc.. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Skin Irritations and Itch Relief (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 (12X, 30X, 1LM), Rhus tox, Selenium metallicum, Sulphur and Urtica urens.).
What is the active ingredient?: Amanita muscaria fruiting body, Aluminum oxide, Lysimachia arvensis whole, Antimony potassium tartrate, Apis mellifera, Arsenic trioxide, Arsenic triiodide, Lycoperdon utriforme fruiting body, Causticum, Mucuna pruriens fruit trichome, Fagopyrum esculentum whole, Graphite, Potassium chloride, Hydrochloric acid, Nerium oleander leaf, Liquid petroleum, Pine tar, Radium bromide, Toxicodendron pubescens leaf, Selenium, Sulfur, Urtica urens whole.
Who is the labeler?: King Bio Inc., NDC labeler code 57955. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Skin Irritations and Itch Relief?: None: this is the only finished product listed under this name.
Is there a related HCPCS / J-code?: Not in Med-Code's curated HCPCS directory. See Billing references above.