Equaline congestion relief NDC 41163-158

NDC codes

FDA NDC Directory

Product NDC (as listed)41163-158Labeler and product segments. Claims need a package NDC.

Product NDC at billing width41163-0158Add 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
41163-158-60	41163015860	20 BLISTER PACK in 1 CARTON (41163-158-60) / 1 TABLET, FILM COATED in 1 BLISTER PACKMarketed from Mar 8, 2021

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): Equaline congestion relief
Generic name (nonproprietary): ibuprofen, phenylephrine hcl
Active ingredients: Ibuprofen — 200 mg/1Phenylephrine hydrochloride — 10 mg/1
Dosage form: Tablet, Film coated
Route: Oral
Labeler: United Natural Foods, Inc. dba UNFI
Product type: Over-the-counter drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 203200
Marketing start: Jul 17, 2015
Listing expires: Dec 31, 2026
Other FDA classes: Adrenergic alpha1-Agonists (Mechanism)Non-Steroidal (Chemical structure)Cyclooxygenase Inhibitors (Mechanism)
Identifiers: Product ID 41163-158_dce4f370-16bd-4192-ab5c-bd74632c1c25SPL ID dce4f370-16bd-4192-ab5c-bd74632c1c25SPL set ID 06dcece5-0fdc-4ff1-a8b1-fadb503a9f50RxCUI 1369775UNII WK2XYI10QM, 04JA59TNSJ
Pharmacologic class: Nonsteroidal Anti-inflammatory Drug; alpha-1 Adrenergic Agonist

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

NDC on a medical claim

N441163015860 followed by a unit qualifier and the quantity

Package 41163-0158-60. 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 Aug 8, 2023.

Indications (excerpt from the label)

Uses • temporarily relieves these symptoms associated with the common cold or flu: • headache • fever • sinus pressure • nasal congestion • minor body aches and pains • reduces swelling of the nasal passages • temporarily restores freer breathing through the nose

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

Other NDCs under ANDA 203200

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

FDA NDC Directory listings under ANDA 203200
Product	Strength	Form · route	Labeler	Product NDC
Congestion Reliefibuprofen, phenylephrine hcl	Ibuprofen 200 mg/1; Phenylephrine hydrochloride 10 mg/1	Tablet, Film coatedOral	Meijer Distribution Inc	41250-158
Sudafed PE Head Congestion Plus Painibuprofen and phenylephrine hydrochloride	Ibuprofen 200 mg/1; Phenylephrine hydrochloride 10 mg/1	Tablet, Film coatedOral	Kenvue Brands LLC	50580-436