Eczema Relief NDC 66096-192

NDC codes

FDA NDC Directory

Product NDC (as listed)66096-192Labeler and product segments. Claims need a package NDC.

Product NDC at billing width66096-0192Add 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
66096-192-05	66096019205	59 mL in 1 PACKAGE (66096-192-05)Marketed from May 22, 2015

How the 11-digit form is made: The product segment has 3 digits, so one leading zero is added to it (5-3-2 → 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): Eczema Relief
Generic name (nonproprietary): arsenicum iodatum, kali bromatum, kali muriaticum, natrum bromatum, niccolum sulphuricum, sulphur iodatum, viola tricolor, zincum bromatum.
Active ingredients: Arsenic triiodide — 8 [hp_X]/59mLPotassium bromide — 4 [hp_X]/59mLPotassium chloride — 4 [hp_X]/59mLSodium bromide — 4 [hp_X]/59mLNickel sulfate hexahydrate — 5 [hp_X]/59mLSulfur iodide — 14 [hp_X]/59mLViola tricolor — 12 [hp_X]/59mLZinc bromide — 6 [hp_X]/59mL
Dosage form: Liquid
Route: Oral
Labeler: OHM PHARMA INC.
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: May 22, 2015
Listing expires: Dec 31, 2026
Other FDA classes: Decreased Copper Ion Absorption (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 66096-192_d44acb83-411f-5445-e053-2995a90a6760SPL ID d44acb83-411f-5445-e053-2995a90a6760SPL set ID 92077b39-ed44-4d73-865f-0ec83e994940UNII 3029988O2T, OSD78555ZM, 660YQ98I10, LC1V549NOM, JC9WZ4FK68, L6L8KA2AA0, 9Q24RAI43V, OO7ZBU9703UPC 0366096192051
Pharmacologic class: Copper Absorption Inhibitor; Osmotic Laxative; Potassium Salt

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

N466096019205 followed by a unit qualifier and the quantity

Package 66096-0192-05. 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 Dec 29, 2021.

Indications (excerpt from the label)

USES: Temporarily relieves eczema - psoriatic skin symptoms.** **This statement has not been evaluated by the FDA. It is based on documented Homeopathic Materia Medica.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)