NDC codes

FDA NDC Directory
Product NDC (as listed)41366-056Labeler and product segments. Claims need a package NDC.
Product NDC at billing width41366-0056Add 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
41366-056-0141366005601259 mL in 1 BOTTLE (41366-056-01)Marketed from Apr 18, 2022

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)
Foaming Hand
Generic name (nonproprietary)
foaming hand soap
Active ingredients
Cocoyl methyl monoethanolamine — 1.2 g/100mLLauramidopropyl betaine — 5 g/100mL
Dosage form
Liquid
Route
Extracorporeal
Labeler
Zhejiang Meimi Technology Co., Ltd.NDC labeler code 41366
Product type
Over-the-counter drug
Marketing category
Unapproved drug (other)
Marketing start
Listing expires
Identifiers
Product ID 41366-056_4545e265-6490-48b4-e063-6294a90abe90SPL ID 4545e265-6490-48b4-e063-6294a90abe90SPL set ID dd009a47-b08a-3788-e053-2995a90aa1ecUNII 79G1T427CF, 23D6XVI233UPC 0049696878876

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 drug-specific HCPCS code in Med-Code's directory for this product. The directory is curated and not complete — check the current CMS HCPCS file before billing.

NDC on a medical claim

N441366005601 followed by a unit qualifier and the quantity

Package 41366-0056-01. 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 .

Indications (excerpt from the label)

APPLYASMALL AMOUNT ONTO WET HANDS. WORK INTO A LATHER AND RINSE.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 41366-056

What is NDC 41366-056?
41366-056 is the product NDC for Foaming Hand (foaming hand soap), Cocoyl methyl monoethanolamine 1.2 g/100mL; Lauramidopropyl betaine 5 g/100mL liquid, listed with the FDA by Zhejiang Meimi Technology Co., Ltd.. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
Foaming Hand (Foaming Hand Soap).
What is the active ingredient?
Cocoyl methyl monoethanolamine, Lauramidopropyl betaine.
Who is the labeler?
Zhejiang Meimi Technology Co., Ltd., NDC labeler code 41366. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Foaming Hand?
4 other product NDCs are listed under this name. See all Foaming Hand NDCs.
Is there a related HCPCS / J-code?
Not in Med-Code's curated HCPCS directory. See Billing references above.

Other finished products listed under the same name: strengths, forms and labelers.

Other Foaming Hand NDCs
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
Foaming Handbenzalkonium chlorideBenzalkonium chloride 1.3 mg/mLSoapTopicalVeritiv Operating Company71897-22471897-0224-86
Foaming Handbenzalkonium chlorideBenzalkonium chloride 1.3 mg/mLSoapTopicalUpLift Brands, LLC83986-22483986-0224-0883986-0224-4583986-0224-86
Foaming Handbenzalkonium chlorideBenzalkonium chloride 1.3 mg/mLLotionTopicalCintas Corporation42961-22442961-0224-71
Foaming Handbenzalkonium chlorideBenzalkonium chloride 1.3 mg/mLLotionTopicalNice-Pak Products, LLC11344-22411344-0224-0811344-0224-4511344-0224-86

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