Eczema Control NDC 51393-5622

NDC codes

FDA NDC Directory

Product NDC (as listed)51393-5622Labeler and product segments. Claims need a package NDC.

Product NDC at billing width51393-5622Add 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
51393-5622-1	51393562201	11 mL in 1 BOTTLE, DISPENSING (51393-5622-1)Marketed from Dec 1, 2011
51393-5622-2	51393562202	33 mL in 1 BOTTLE, DISPENSING (51393-5622-2)Marketed from Dec 1, 2011
51393-5622-3	51393562203	30 mL in 1 BOTTLE, DROPPER (51393-5622-3)Marketed from Aug 1, 2021
51393-5622-5	51393562205	5 mL in 1 BOTTLE, DISPENSING (51393-5622-5)Marketed from Jul 1, 2016

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 Control
Generic name (nonproprietary): centella asiatica, iris versicolor root, arctium lappa root, sodium chloride, ruta graveolens flowering top, silicon dioxide, taraxacum officinale, and thuja occidentalis root
Active ingredients: Centella asiatica whole — 12 [hp_C]/100mLIris versicolor root — 12 [hp_C]/100mLArctium lappa root — 12 [hp_C]/100mLSodium chloride — 12 [hp_X]/100mLRuta graveolens flowering top — 12 [hp_C]/100mLSilicon dioxide — 6 [hp_X]/100mLTaraxacum officinale — 6 [hp_C]/100mLThuja occidentalis root — 8 [hp_X]/100mL
Dosage form: Solution/ drops
Route: Topical
Labeler: Forces of Nature
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Dec 1, 2011
Listing expires: Dec 31, 2027
Identifiers: Product ID 51393-5622_5bb3baba-b95c-a2f0-e063-6394a90a98b7SPL ID 5bb3baba-b95c-a2f0-e063-6394a90a98b7

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. Topical products like this are usually dispensed by a pharmacy and billed by NDC.

NDC on a medical claim

N451393562201 followed by a unit qualifier and the quantity

Package 51393-5622-01. 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

The FDA listing for this product does not reference a label (SPL) set.