NDC codes

FDA NDC Directory
Product NDC (as listed)84725-001Labeler and product segments. Claims need a package NDC.
Product NDC at billing width84725-0001Add 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 NDC11-digit (billing)PackageCopy
84725-001-01847250001011 TUBE in 1 PACKAGE (84725-001-01) / 2 g in 1 TUBEMarketed from Sep 8, 2026
84725-001-02847250001021 BOTTLE, PUMP in 1 PACKAGE (84725-001-02) / 2 g in 1 BOTTLE, PUMPMarketed from Sep 8, 2026

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)
Docosanol
Generic name (nonproprietary)
docosanol
Active ingredients
Docosanol — 100 mg/g
Dosage form
Cream
Route
Topical
Product type
Over-the-counter drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 220017
Marketing start
Listing expires
Identifiers
Product ID 84725-001_7a974299-b61c-4d18-b795-06aeda87b0c4SPL ID 7a974299-b61c-4d18-b795-06aeda87b0c4SPL set ID 5783edbf-2ce6-4b7e-8df3-2e421c63d0e8RxCUI 797534UNII 9G1OE216XYUPC 0384725001017, 0384725001024

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

N484725000101 followed by a unit qualifier and the quantity

Package 84725-0001-01. 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

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