NDC codes

FDA NDC Directory
Product NDC (as listed)72162-2203Labeler and product segments. Claims need a package NDC.
Product NDC at billing width72162-2203Add 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
72162-2203-4721622203047216222030485 g in 1 BOTTLE (72162-2203-4)Marketed from Dec 19, 2023
72162-2203-7721622203077216222030728.35 g in 1 BOTTLE (72162-2203-7)Marketed from Dec 19, 2023
72162-2203-87216222030872162220308198.4 g in 1 BOTTLE (72162-2203-8)Marketed from Dec 19, 2023

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 Percent
Generic name (nonproprietary)
urea
Active ingredients
Urea — 400 mg/g
Dosage form
Cream
Route
Topical
Labeler
Bryant Ranch PrepackNDC labeler code 72162
Product type
Prescription drug
Marketing category
Unapproved drug (other)
Marketing start
Listing expires
Identifiers
Product ID 72162-2203_47c029cd-a0dc-45a7-a91f-729889bcf007SPL ID 47c029cd-a0dc-45a7-a91f-729889bcf007SPL set ID e28969bc-c3a0-49e5-9947-aee0c6b8b0b5RxCUI 198342UNII 8W8T17847W

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

N472162220304 followed by a unit qualifier and the quantity

Package 72162-2203-04. 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 eschar. 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 72162-2203

What is NDC 72162-2203?
72162-2203 is the product NDC for Urea Cream 40 Percent (urea), Urea 400 mg/g cream, listed with the FDA by Bryant Ranch Prepack. It has 3 package NDCs, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
Urea Cream 40 Percent (Urea).
What is the active ingredient?
Urea.
Who is the labeler?
Bryant Ranch Prepack, NDC labeler code 72162. 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 Percent?
2 other product NDCs are listed under this name. See all Urea Cream 40 Percent 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 Percent NDCs
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
Urea Cream 40 PercentureaUrea 400 mg/gCreamTopicalMethod Pharmaceuticals, LLC58657-48958657-0489-0158657-0489-0358657-0489-07
Urea Cream 40 PercentureaUrea 400 mg/gCreamTopicalBryant Ranch Prepack71335-286871335-2868-01

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