All Day Back and Muscle Pain Relief NDC 79903-609

NDC codes

FDA NDC Directory

Product NDC (as listed)79903-609Labeler and product segments. Claims need a package NDC.

Product NDC at billing width79903-0609Add 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
79903-609-09	79903060909	1 BOTTLE in 1 CARTON (79903-609-09) / 90 TABLET, COATED in 1 BOTTLEMarketed from Dec 15, 2023
79903-609-20	79903060920	1 BOTTLE in 1 CARTON (79903-609-20) / 200 TABLET, COATED in 1 BOTTLEMarketed from Dec 15, 2023

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): All Day Back and Muscle Pain Relief
Generic name (nonproprietary): naproxen sodium
Active ingredients: Naproxen sodium — 220 mg/1
Dosage form: Tablet, Coated
Route: Oral
Labeler: Walmart Inc.
Product type: Over-the-counter drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 090545
Marketing start: Dec 15, 2023
Listing expires: Dec 31, 2026
Other FDA classes: Non-Steroidal (Chemical structure)Cyclooxygenase Inhibitors (Mechanism)
Identifiers: Product ID 79903-609_0bafa4ac-8c2d-006b-e063-6294a90ab1fcSPL ID 0bafa4ac-8c2d-006b-e063-6294a90ab1fcSPL set ID 062b9ffe-b4fc-9f5a-e063-6294a90a560eRxCUI 849574UNII 9TN87S3A3CUPC 0194346189106, 0194346189113
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

N479903060909 followed by a unit qualifier and the quantity

Package 79903-0609-09. 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 4, 2023.

Indications (excerpt from the label)

Uses temporarily relieves minor aches and pains 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	Tablet, CoatedOral	WALGREENS	0363-6099
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
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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