What is NDC 71399-0480?

71399-0480 is the product NDC for Sodium Sulfacetamide, Sulfacetamide sodium 100 mg/mL liquid, listed with the FDA by Akron Pharma Inc. It has 3 package NDCs, shown above in 10- and 11-digit form.

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 Sodium Sulfacetamide?

13 other product NDCs are listed under this name.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

Sodium Sulfacetamide NDC 71399-0480

NDC codes

FDA NDC Directory

Product NDC (as listed)71399-0480Labeler and product segments. Claims need a package NDC.

Product NDC at billing width71399-0480Add 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
71399-0480-2	7139904800271399048002	360 mL in 1 BOTTLE (71399-0480-2)Marketed from Sep 13, 2024
71399-0480-6	7139904800671399048006	480 mL in 1 BOTTLE (71399-0480-6)Marketed from Sep 13, 2024
71399-0480-8	7139904800871399048008	240 mL in 1 BOTTLE (71399-0480-8)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): Sodium Sulfacetamide
Generic name (nonproprietary): sodium sulfacetamide
Active ingredients: Sulfacetamide sodium — 100 mg/mL
Dosage form: Liquid
Route: Topical
Labeler: Akron Pharma IncNDC labeler code 71399
Product type: Prescription drug
Marketing category: Unapproved drug (other)
Marketing start: Sep 13, 2024
Listing expires: Dec 31, 2026
Other FDA classes: Sulfonamides (Chemical structure)
Identifiers: Product ID 71399-0480_fd982d15-1435-4bbf-a29f-71e8bdd4eb2fSPL ID fd982d15-1435-4bbf-a29f-71e8bdd4eb2fSPL set ID ba08bf7c-5fdc-447a-b8de-3f319cee7e4eRxCUI 1006107UNII 4NRT660KJQUPC 0371399048066
Pharmacologic class: Sulfonamide Antibacterial

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

N471399048002 followed by a unit qualifier and the quantity

Package 71399-0480-02. 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 Sep 24, 2024.

Indications (excerpt from the label)

INDICATIONS: This product is intended for topical application in the following scaling dermatoses: seborrheic dermatitis and seborrhea sicca (dandruff). It also is indicated for the treatment of secondary bacterial infections of the skin due to organisms susceptible to sulfonamides.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 71399-0480

What is NDC 71399-0480?: 71399-0480 is the product NDC for Sodium Sulfacetamide, Sulfacetamide sodium 100 mg/mL liquid, 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?: Sodium Sulfacetamide.
What is the active ingredient?: Sulfacetamide sodium.
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 Sodium Sulfacetamide?: 13 other product NDCs are listed under this name. See all Sodium Sulfacetamide 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 Sodium Sulfacetamide NDCs
Product	Strength	Form · route	Labeler	Product NDC	Package NDCs (11-digit)
Sodium Sulfacetamide	Sulfacetamide sodium 100 mg/mL	ShampooTopical	Akron Pharma Inc	71399-1599	71399-1599-08
Sodium Sulfacetamide	Sulfacetamide sodium 100 mg/mL	ShampooTopical	Laser Pharmaceuticals, LLC	16477-411	16477-0411-08
Sodium Sulfacetamide	Sulfacetamide sodium 100 mg/g	LiquidTopical	Method Pharmaceuticals, LLC	58657-477	58657-0477-0658657-0477-1258657-0477-16
Sodium Sulfacetamide	Sulfacetamide sodium 100 mg/g	LiquidTopical	Bryant Ranch Prepack	63629-9262	63629-9262-01
Sodium Sulfacetamide	Sulfacetamide sodium 100 mg/g	LiquidTopical	Bryant Ranch Prepack	63629-9263	63629-9263-01
Sodium Sulfacetamide	Sulfacetamide sodium 100 mg/g	LiquidTopical	Bryant Ranch Prepack	63629-9264	63629-9264-01
Sodium Sulfacetamide	Sulfacetamide sodium 100 mg/g	LiquidTopical	Bryant Ranch Prepack	72162-1665	72162-1665-0272162-1665-0472162-1665-07
Sodium Sulfacetamide	Sulfacetamide sodium 100 mg/mL	LiquidTopical	Laser Pharmaceuticals, LLC	16477-410	16477-0410-0616477-0410-12
Sodium sulfacetamide	Sulfacetamide sodium 100 mg/mL	LotionTopical	Oceanside Pharmaceuticals	68682-010	68682-0010-04
Sodium Sulfacetamide	Sulfacetamide sodium 100 mg/mL	LiquidTopical	BioComp Pharma, Inc.	44523-606	44523-0606-1244523-0606-16

All 14 Sodium Sulfacetamide NDCs