Sodium sulfacetamide NDC 68682-010

NDC codes

FDA NDC Directory

Product NDC (as listed)68682-010Labeler and product segments. Claims need a package NDC.

Product NDC at billing width68682-0010Add 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
68682-010-04	68682001004	1 BOTTLE, PLASTIC in 1 CARTON (68682-010-04) / 118 mL in 1 BOTTLE, PLASTICMarketed from Dec 18, 2015

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): Sodium sulfacetamide
Generic name (nonproprietary): sodium sulfacetamide
Active ingredients: Sulfacetamide sodium — 100 mg/mL
Dosage form: Lotion
Route: Topical
Labeler: Oceanside Pharmaceuticals
Product type: Prescription drug
Marketing category: NDA authorized genericApplication NDA 019931
Marketing start: Dec 18, 2015
Listing expires: Dec 31, 2026
Other FDA classes: Sulfonamides (Chemical structure)
Identifiers: Product ID 68682-010_4dcab06b-56fb-4e42-aae0-6e8840ddd80aSPL ID 4dcab06b-56fb-4e42-aae0-6e8840ddd80aSPL set ID 6fa7399b-4ced-492d-b6f6-cf155764087aRxCUI 1006688UNII 4NRT660KJQ
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

N468682001004 followed by a unit qualifier and the quantity

Package 68682-0010-04. 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 May 31, 2019.

Indications (excerpt from the label)

INDICATIONS Sodium Sulfacetamide Lotion is indicated in the topical treatment of acne vulgaris .

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

Other NDCs under NDA 019931

Products listed under the same FDA application: other strengths and forms, and repackagers who relabel the same product.

FDA NDC Directory listings under NDA 019931
Product	Strength	Form · route	Labeler	Product NDC
Klaronsulfacetamide sodium	Sulfacetamide sodium 100 mg/mL	LotionTopical	Bausch Health US, LLC	0187-5198