NDC codes

FDA NDC Directory
Product NDC (as listed)42681-0058Labeler and product segments. Claims need a package NDC.
Product NDC at billing width42681-0058Add 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
42681-0058-1426810058011 BOTTLE in 1 CARTON (42681-0058-1) / 60 SPRAY, METERED in 1 BOTTLEMarketed from Jan 22, 2026

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)
365 Whole Foods Market Fluticasone Propionate
Generic name (nonproprietary)
fluticasone propionate
Active ingredients
Fluticasone propionate — 50 ug/1
Dosage form
Spray, Metered
Route
Nasal
Product type
Over-the-counter drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 217088
Marketing start
Listing expires
Other FDA classes
Corticosteroid Hormone Receptor Agonists (Mechanism)
Identifiers
Product ID 42681-0058_313517bd-cb08-49a5-8ef1-e5522cc21c80SPL ID 313517bd-cb08-49a5-8ef1-e5522cc21c80SPL set ID 313517bd-cb08-49a5-8ef1-e5522cc21c80RxCUI 1797907UNII O2GMZ0LF5W
Pharmacologic class
Corticosteroid

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. Nasal products like this are usually dispensed by a pharmacy and billed by NDC.

NDC on a medical claim

N442681005801 followed by a unit qualifier and the quantity

Package 42681-0058-01. 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)

Uses Temporarily relieves these symptoms of hay fever or other upper respiratory allergies: nasal congestion itchy, watery eyes itchy nose runny nose sneezing

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

Other NDCs under ANDA 217088

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

FDA NDC Directory listings under ANDA 217088
ProductStrengthForm · routeLabelerProduct NDC
Fluticarefluticasone propionateFluticasone propionate 50 ug/1Spray, MeteredNasalINNOVUS PHARMACEUTICALS, INC.57483-180
Mucinex Nasal Congestion and Allergy Relieffluticasone propionateFluticasone propionate 50 ug/1Spray, MeteredNasalReckitt Benckiser LLC72854-227
Fluticasone PropionateFluticasone propionate 50 ug/1Spray, MeteredNasalAurohealth LLC58602-017
Childrens Fluticasone Propionatefluticasone propionateFluticasone propionate 50 ug/1Spray, MeteredNasalAurohealth LLC58602-018
Fluticasone PropionateFluticasone propionate 50 ug/1Spray, MeteredNasalFamily Dollar Stores, LLC55319-058
Fluticasone PropionateFluticasone propionate 50 ug/1Spray, MeteredNasalYYBA Corp73581-510

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