NDC codes

FDA NDC Directory
Product NDC (as listed)71399-8456Labeler and product segments. Claims need a package NDC.
Product NDC at billing width71399-8456Add 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
71399-8456-1713998456017139984560128.35 g in 1 BOTTLE (71399-8456-1)Marketed from Sep 13, 2024
71399-8456-3713998456037139984560385 g in 1 BOTTLE (71399-8456-3)Marketed from Sep 13, 2024
71399-8456-77139984560771399845607198.45 g in 1 BOTTLE (71399-8456-7)Marketed from Sep 13, 2024

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)
Urea Cream 40%
Generic name (nonproprietary)
urea
Active ingredients
Urea — 400 mg/g
Dosage form
Cream
Route
Topical
Labeler
Akron Pharma Inc.NDC labeler code 71399
Product type
Prescription drug
Marketing category
Unapproved drug (other)
Marketing start
Listing expires
Identifiers
Product ID 71399-8456_6153c0bc-1246-4396-a26d-cd066b909ef5SPL ID 6153c0bc-1246-4396-a26d-cd066b909ef5SPL set ID 0ce643e9-cf13-4b51-8ffd-8d5636d73e51RxCUI 198342UNII 8W8T17847WUPC 0371399845672, 0371399845634, 0371399845610

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

N471399845601 followed by a unit qualifier and the quantity

Package 71399-8456-01. 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)

Indications and Usage For debridement and promotion of normal healing of hyperkeratotic surface lesions, particularly where healing is retarded by local infection, necrotic tissue, fibrinous or purulent debris or eshar. Urea is useful for the treatment of hyperkeratotic conditions such as dry, rough skin, dermatitis, psoriasis, xerosis, ichthyosis, eczema, keratosis pilaris, keratosis palmaris, keratoderma, corns and calluses, as well as damaged, ingrown and devitalized nails.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 71399-8456

What is NDC 71399-8456?
71399-8456 is the product NDC for Urea Cream 40% (urea), Urea 400 mg/g cream, listed with the FDA by Akron Pharma Inc.. It has 3 package NDCs, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
Urea Cream 40% (Urea).
What is the active ingredient?
Urea.
Who is the labeler?
Akron Pharma Inc., NDC labeler code 71399. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Urea Cream 40%?
1 other product NDC are listed under this name. See all Urea Cream 40% 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 Urea Cream 40% NDCs
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
Urea Cream 40%ureaUrea 400 mg/gCreamTopicalLaser Pharmaceuticals, LLC16477-34016477-0340-0116477-0340-0316477-0340-07

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