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 NDC11-digit (billing)PackageCopy
51393-5622-1513935622015139356220111 mL in 1 BOTTLE, DISPENSING (51393-5622-1)Marketed from Dec 1, 2011
51393-5622-2513935622025139356220233 mL in 1 BOTTLE, DISPENSING (51393-5622-2)Marketed from Dec 1, 2011
51393-5622-3513935622035139356220330 mL in 1 BOTTLE, DROPPER (51393-5622-3)Marketed from Aug 1, 2021
51393-5622-551393562205513935622055 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 NatureNDC labeler code 51393
Product type
Over-the-counter drug
Marketing category
Unapproved homeopathic
Marketing start
Listing expires
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.

About NDC 51393-5622

What is NDC 51393-5622?
51393-5622 is the product NDC for Eczema Control, Centella asiatica whole 12 [hp_C]/100mL + 7 more ingredients solution/ drops, listed with the FDA by Forces of Nature. It has 4 package NDCs, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
Eczema Control (Centella Asiatica, Iris Versicolor Root, Arctium Lappa Root, Sodium Chloride, Ruta Graveolens Flowering Top, Silicon Dioxide, Taraxacum Officinale, and Thuja Occidentalis Root).
What is the active ingredient?
Centella asiatica whole, Iris versicolor root, Arctium lappa root, Sodium chloride, Ruta graveolens flowering top, Silicon dioxide, Taraxacum officinale, Thuja occidentalis root.
Who is the labeler?
Forces of Nature, NDC labeler code 51393. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Eczema Control?
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.

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