All Day Pain Relief (naproxen sodium) NDC 0363-6099

NDC codes

FDA NDC Directory

Product NDC (as listed)0363-6099Labeler and product segments. Claims need a package NDC.

Product NDC at billing width00363-6099Add 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
0363-6099-01	00363609901	100 TABLET, COATED in 1 BOTTLE (0363-6099-01)Marketed from Jul 8, 2019
0363-6099-05	00363609905	50 TABLET, COATED in 1 BOTTLE (0363-6099-05)Marketed from Jul 8, 2019
0363-6099-20	00363609920	200 TABLET, COATED in 1 BOTTLE (0363-6099-20)Marketed from Jul 8, 2019

How the 11-digit form is made: The labeler segment has 4 digits, so one leading zero is added to it (4-4-2 → 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): All Day Pain Relief
Generic name (nonproprietary): naproxen sodium
Active ingredients: Naproxen sodium — 220 mg/1
Dosage form: Tablet, Coated
Route: Oral
Labeler: WALGREENS
Product type: Over-the-counter drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 090545
Marketing start: Jun 30, 2019
Listing expires: Dec 31, 2026
Other FDA classes: Non-Steroidal (Chemical structure)Cyclooxygenase Inhibitors (Mechanism)
Identifiers: Product ID 0363-6099_13b172b6-b829-8fe5-e063-6294a90a37e3SPL ID 13b172b6-b829-8fe5-e063-6294a90a37e3SPL set ID 8771300f-e907-3d53-e053-2a95a90ae402RxCUI 849574UNII 9TN87S3A3C
Pharmacologic class: Nonsteroidal Anti-inflammatory Drug

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

N400363609901 followed by a unit qualifier and the quantity

Package 00363-6099-01. 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 Mar 15, 2024.

Indications (excerpt from the label)

temporarily relieves minor aches and pain due to: minor pain of arthritis muscular aches backache menstrual cramps headache toothache the common cold temporarily reduces fever

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

Other NDCs under ANDA 090545

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

FDA NDC Directory listings under ANDA 090545
Product	Strength	Form · route	Labeler	Product NDC
Flanax Pain Reliever/Fever Reducernaproxen sodium	Naproxen sodium 220 mg/1	TabletOral	Navajo Manufacturing Company Inc.	67751-125
Pain Reliefnaproxen sodium	Naproxen sodium 220 mg/1	TabletOral	BETTER LIVING BRANDS, LLC	21130-608
All Day Pain Reliefnaproxen sodium	Naproxen sodium 220 mg/1	Tablet, CoatedOral	WALGREENS	0363-9608
Naproxen Caplets All day relief for painnaproxen sodium 220 mg	Naproxen sodium 220 mg/1	TabletOral	Allegiant Health	69168-362
Naproxen Capletsnaproxen sodium 220 mg	Naproxen sodium 220 mg/1	TabletOral	Allegiant Health	69168-394
Back And Muscle Painnaproxen	Naproxen sodium 220 mg/1	Tablet, CoatedOral	WALGREENS	0363-9609
Naproxen Sodium 220mg	Naproxen sodium 220 mg/1	Tablet, CoatedOral	Allegiant Health	69168-395
Naproxen Sodium	Naproxen sodium 220 mg/1	TabletOral	BETTER LIVING BRANDS LLC.	21130-690
Calmadol Pain Relievernaproxen sodium	Naproxen sodium 220 mg/1	TabletOral	GRANDALL DISTRIBUTING, LLC	48201-007
Naproxen Sodiumnaproxen sodium tablet, coated	Naproxen sodium 220 mg/1	TabletOral	MARKSANS PHARMA LIMITED	25000-144
All Day Pain Reliefnaproxen sodium	Naproxen sodium 220 mg/1	TabletOral	Walmart Inc.	79903-389
Naproxen Sodiumnaproxen sodium, coated tablets	Naproxen sodium 220 mg/1	TabletOral	MARKSANS PHARMA LIMITED	25000-141
Naproxen Sodium 220mg	Naproxen sodium 220 mg/1	Tablet, CoatedOral	Command Brands, LLC	69197-394
All Day Back and Muscle Pain Reliefnaproxen sodium	Naproxen sodium 220 mg/1	Tablet, CoatedOral	Walmart Inc.	79903-609
Naproxen Sodium 220mg	Naproxen sodium 220 mg/1	Tablet, Film coatedOral	Grocery Outlet	85828-394
Naproxen Sodium 220mg	Naproxen sodium 220 mg/1	Tablet, CoatedOral	Athlete's Needs, Inc.	53185-394
Naproxen Sodiumnaproxen sodium 220mg	Naproxen sodium 220 mg/1	TabletOral	CVS Pharmacy, Inc.	51316-608
Naproxen Sodium	Naproxen sodium 220 mg/1	Tablet, CoatedOral	Kroger Company	41226-609
Naproxen Sodium	Naproxen sodium 220 mg/1	Tablet, Film coatedOral	TIME CAP LABORATORIES, INC	49483-608
Naproxen Sodium	Naproxen sodium 220 mg/1	Tablet, Film coatedOral	TIME CAP LABORATORIES, INC	49483-609

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