What is NDC 72944-0001?

72944-0001 is the product NDC for Kenaf wet wipe (allantoin), Allantoin .05 g/100g liquid, listed with the FDA by MEDICELL BIO CO., Ltd.. It has 1 package NDC, shown above in 10- and 11-digit form.

MEDICELL BIO CO., Ltd., NDC labeler code 72944. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.

What other NDCs exist for Kenaf wet wipe?

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.

Kenaf wet wipe NDC 72944-0001 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)72944-0001Labeler and product segments. Claims need a package NDC.

Product NDC at billing width72944-0001Add 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
72944-0001-1	7294400010172944000101	190 g in 1 POUCH (72944-0001-1)Marketed from Apr 9, 2017

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): Kenaf wet wipe
Generic name (nonproprietary): allantoin
Active ingredients: Allantoin — .05 g/100g
Dosage form: Liquid
Route: Topical
Labeler: MEDICELL BIO CO., Ltd.NDC labeler code 72944
Product type: Over-the-counter drug
Marketing category: Unapproved drug (other)
Marketing start: Apr 9, 2017
Listing expires: Dec 31, 2026
Identifiers: Product ID 72944-0001_384bb90a-444d-547a-e063-6394a90a354bSPL ID 384bb90a-444d-547a-e063-6394a90a354bSPL set ID 860f9cc5-a00e-7ccf-e053-2a91aa0a0782UNII 344S277G0Z

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

N472944000101 followed by a unit qualifier and the quantity

Package 72944-0001-01. 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 Jun 24, 2025.

Indications (excerpt from the label)

Apply to skin and wipe

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 72944-0001

What is NDC 72944-0001?: 72944-0001 is the product NDC for Kenaf wet wipe (allantoin), Allantoin .05 g/100g liquid, listed with the FDA by MEDICELL BIO CO., Ltd.. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Kenaf wet wipe (Allantoin).
What is the active ingredient?: Allantoin.
Who is the labeler?: MEDICELL BIO CO., Ltd., NDC labeler code 72944. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Kenaf wet wipe?: 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.

Kenaf wet wipe (Allantoin) NDC 72944-0001