What is NDC 58602-018?

58602-018 is the product NDC for Childrens Fluticasone Propionate (fluticasone propionate), Fluticasone propionate 50 ug/1 spray, metered, listed with the FDA by Aurohealth LLC. It has 4 package NDCs, shown above in 10- and 11-digit form.

What drug is associated with this NDC?

Childrens Fluticasone Propionate (Fluticasone propionate).

Aurohealth LLC, NDC labeler code 58602. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.

What other NDCs exist for Childrens Fluticasone Propionate?

None: this is the only finished product listed under this name.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

Childrens Fluticasone Propionate NDC 58602-018

NDC codes

FDA NDC Directory

Product NDC (as listed)58602-018Labeler and product segments. Claims need a package NDC.

Product NDC at billing width58602-0018Add 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
58602-018-04	5860200180458602001804	3 BOTTLE in 1 CARTON (58602-018-04) / 72 SPRAY, METERED in 1 BOTTLEMarketed from Dec 16, 2025
58602-018-42	5860200184258602001842	1 BOTTLE in 1 CARTON (58602-018-42) / 60 SPRAY, METERED in 1 BOTTLEMarketed from May 10, 2024
58602-018-45	5860200184558602001845	2 BOTTLE in 1 CARTON (58602-018-45) / 72 SPRAY, METERED in 1 BOTTLEMarketed from Dec 16, 2025
58602-018-51	5860200185158602001851	1 BOTTLE in 1 CARTON (58602-018-51) / 72 SPRAY, METERED in 1 BOTTLEMarketed from Dec 16, 2025

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): Childrens Fluticasone Propionate
Generic name (nonproprietary): fluticasone propionate
Active ingredients: Fluticasone propionate — 50 ug/1
Dosage form: Spray, Metered
Route: Nasal
Labeler: Aurohealth LLCNDC labeler code 58602
Product type: Over-the-counter drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 217088
Marketing start: May 10, 2024
Listing expires: Dec 31, 2027
Other FDA classes: Corticosteroid Hormone Receptor Agonists (Mechanism)
Identifiers: Product ID 58602-018_0bdbc9dc-56d3-478b-97bc-7e8a43d200b0SPL ID 0bdbc9dc-56d3-478b-97bc-7e8a43d200b0SPL set ID 180ef101-dca6-496f-8376-63449d82d083RxCUI 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

N458602001804 followed by a unit qualifier and the quantity

Package 58602-0018-04. 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 Dec 8, 2025.

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)

About NDC 58602-018

What is NDC 58602-018?: 58602-018 is the product NDC for Childrens Fluticasone Propionate (fluticasone propionate), Fluticasone propionate 50 ug/1 spray, metered, listed with the FDA by Aurohealth LLC. It has 4 package NDCs, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Childrens Fluticasone Propionate (Fluticasone propionate).
What is the active ingredient?: Fluticasone propionate.
Who is the labeler?: Aurohealth LLC, NDC labeler code 58602. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Childrens Fluticasone Propionate?: None: this is the only finished product listed under this name.
Is there a related HCPCS / J-code?: Not in Med-Code's curated HCPCS directory. See Billing references above.

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
Product	Strength	Form · route	Labeler	Product NDC
365 Whole Foods Market Fluticasone Propionatefluticasone propionate	Fluticasone propionate 50 ug/1	Spray, MeteredNasal	Whole Foods Market, Inc.	42681-0058
Fluticarefluticasone propionate	Fluticasone propionate 50 ug/1	Spray, MeteredNasal	INNOVUS PHARMACEUTICALS, INC.	57483-180
Fluticasone Propionate	Fluticasone propionate 50 ug/1	Spray, MeteredNasal	Family Dollar Stores, LLC	55319-058
Fluticasone Propionate	Fluticasone propionate 50 ug/1	Spray, MeteredNasal	Aurohealth LLC	58602-017
Fluticasone Propionate	Fluticasone propionate 50 ug/1	Spray, MeteredNasal	YYBA Corp	73581-510
Mucinex Nasal Congestion and Allergy Relieffluticasone propionate	Fluticasone propionate 50 ug/1	Spray, MeteredNasal	Reckitt Benckiser LLC	72854-227

Childrens Fluticasone Propionate (Fluticasone propionate) NDC 58602-018