Eczema HP NDC 43406-0019

NDC codes

FDA NDC Directory

Product NDC (as listed)43406-0019Labeler and product segments. Claims need a package NDC.

Product NDC at billing width43406-0019Add 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
43406-0019-1	43406001901	30 mL in 1 BOTTLE, DROPPER (43406-0019-1)Marketed from May 29, 2007

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): Eczema HP
Generic name (nonproprietary): arsenic trioxide 30x, oyster shell calcium carbonate, crude 30x, graphite 30x, mercurius solubilis 30x, daphne mezereum bark 30x, toxicodendron pubescens leaf 30x, sepia officinalis juice 30x, sulfur 30x
Active ingredients: Arsenic trioxide — 30 [hp_X]/mLOyster shell calcium carbonate, Crude — 30 [hp_X]/mLGraphite — 30 [hp_X]/mLMercurius solubilis — 30 [hp_X]/mLDaphne mezereum bark — 30 [hp_X]/mLToxicodendron pubescens leaf — 30 [hp_X]/mLSepia officinalis juice — 30 [hp_X]/mLSulfur — 30 [hp_X]/mL
Dosage form: Liquid
Route: Oral
Labeler: Natural Creations, Inc.
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: May 29, 2007
Listing expires: Dec 31, 2026
Identifiers: Product ID 43406-0019_899a9516-b5ed-40d2-a044-a2cb4ddbc91aSPL ID 899a9516-b5ed-40d2-a044-a2cb4ddbc91aSPL set ID 725d40fe-e9e4-40ff-8b18-5bd5c3e356f8UNII S7V92P67HO, 2E32821G6I, 4QQN74LH4O, 324Y4038G2, X2N6E405GV, 6IO182RP7A, QDL83WN8C2, 70FD1KFU70

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

N443406001901 followed by a unit qualifier and the quantity

Package 43406-0019-01. 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 Jan 5, 2023.

Indications (excerpt from the label)

USES: Temporarily relieves minor skin irritation due to eczema.**

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)