What is NDC 0113-5299?

0113-5299 is the product NDC for Good Sense Dual Action Back Pain, Acetaminophen 250 mg/1; Ibuprofen 125 mg/1 tablet, film coated, listed with the FDA by L. Perrigo Company. It has 4 package NDCs, shown above in 10- and 11-digit form.

What drug is associated with this NDC?

Good Sense Dual Action Back Pain (Acetaminophen, ibuprofen).

L. Perrigo Company, NDC labeler code 0113. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.

What other NDCs exist for Good Sense Dual Action Back Pain?

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.

Good Sense Dual Action Back Pain NDC 0113-5299

NDC codes

FDA NDC Directory

Product NDC (as listed)0113-5299Labeler and product segments. Claims need a package NDC.

Product NDC at billing width00113-5299Add 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
0113-5299-16	00113529916	1 BOTTLE in 1 CARTON (0113-5299-16) / 144 TABLET, FILM COATED in 1 BOTTLEMarketed from Mar 15, 2024
0113-5299-23	00113529923	1 BOTTLE in 1 CARTON (0113-5299-23) / 72 TABLET, FILM COATED in 1 BOTTLEMarketed from Mar 7, 2024
0113-5299-68	00113529968	1 BOTTLE in 1 CARTON (0113-5299-68) / 36 TABLET, FILM COATED in 1 BOTTLEMarketed from Mar 7, 2024
0113-5299-89	00113529989	1 BOTTLE in 1 CARTON (0113-5299-89) / 18 TABLET, FILM COATED in 1 BOTTLEMarketed from Mar 15, 2024

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): Good Sense Dual Action Back Pain
Generic name (nonproprietary): acetaminophen, ibuprofen
Active ingredients: Acetaminophen — 250 mg/1Ibuprofen — 125 mg/1
Dosage form: Tablet, Film coated
Route: Oral
Labeler: L. Perrigo CompanyNDC labeler code 0113
Product type: Over-the-counter drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 214836
Marketing start: Mar 7, 2024
Listing expires: Dec 31, 2026
Other FDA classes: Non-Steroidal (Chemical structure)Cyclooxygenase Inhibitors (Mechanism)
Identifiers: Product ID 0113-5299_89476188-cf88-4184-a366-ed4c2e7db145SPL ID 89476188-cf88-4184-a366-ed4c2e7db145SPL set ID 89476188-cf88-4184-a366-ed4c2e7db145RxCUI 2387532UNII 362O9ITL9D, WK2XYI10QM
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

N400113529916 followed by a unit qualifier and the quantity

Package 00113-5299-16. 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 19, 2024.

Indications (excerpt from the label)

Uses • temporarily relieves minor aches and pains due to: • backache • muscular aches • minor pain of arthritis • headache • toothache • menstrual cramps

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 0113-5299

What is NDC 0113-5299?: 0113-5299 is the product NDC for Good Sense Dual Action Back Pain, Acetaminophen 250 mg/1; Ibuprofen 125 mg/1 tablet, film coated, listed with the FDA by L. Perrigo Company. It has 4 package NDCs, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Good Sense Dual Action Back Pain (Acetaminophen, ibuprofen).
What is the active ingredient?: Acetaminophen, Ibuprofen.
Who is the labeler?: L. Perrigo Company, NDC labeler code 0113. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Good Sense Dual Action Back Pain?: 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 214836

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

FDA NDC Directory listings under ANDA 214836
Product	Strength	Form · route	Labeler	Product NDC
acetaminophen and ibuprofenacetaminophen, ibuprofen	Acetaminophen 250 mg/1; Ibuprofen 125 mg/1	Tablet, Film coatedOral	Kroger Company	30142-720
Basic Care Dual Actionacetaminophen, ibuprofen	Acetaminophen 250 mg/1; Ibuprofen 125 mg/1	Tablet, Film coatedOral	Amazon.com Services LLC	72288-530
Careone Dual Actionacetaminophen, ibuprofen	Acetaminophen 250 mg/1; Ibuprofen 125 mg/1	Tablet, Film coatedOral	Retail Business Services, LLC	72476-231
dg health dual back pain relieveracetaminophen, ibuprofen	Acetaminophen 250 mg/1; Ibuprofen 125 mg/1	Tablet, Film coatedOral	Dolgencorp Inc	55910-508
DG health dual pain relieveracetaminophen, ibuprofen	Acetaminophen 250 mg/1; Ibuprofen 125 mg/1	Tablet, Film coatedOral	Dolgencorp Inc	55910-441
dual actionacetaminophen, ibuprofen	Acetaminophen 250 mg/1; Ibuprofen 125 mg/1	Tablet, Film coatedOral	Rite Aid Corporation	11822-5777
Dual Actionacetaminophen, ibuprofen	Acetaminophen 250 mg/1; Ibuprofen 125 mg/1	Tablet, Film coatedOral	HyVee Inc	42507-540
dual actionacetaminophen, ibuprofen	Acetaminophen 250 mg/1; Ibuprofen 125 mg/1	Tablet, Film coatedOral	Publix Super Markets Inc	56062-530
Dual Actionacetaminophen, ibuprofen	Acetaminophen 250 mg/1; Ibuprofen 125 mg/1	Tablet, Film coatedOral	Amazon.com Services LLC	72288-542
Dual Action Back Pain Relieveracetaminophen, ibuprofen	Acetaminophen 250 mg/1; Ibuprofen 125 mg/1	Tablet, Film coatedOral	Meijer, Inc.	79481-0152
Dual Back Pain Relieveracetaminophen, ibuprofen	Acetaminophen 250 mg/1; Ibuprofen 125 mg/1	Tablet, Film coatedOral	Walgreen Company	0363-6199
dual pain relieveracetaminophen, ibuprofen	Acetaminophen 250 mg/1; Ibuprofen 125 mg/1	Tablet, Film coatedOral	Walgreen Company	0363-5220
dual pain relieveracetaminophen, ibuprofen	Acetaminophen 250 mg/1; Ibuprofen 125 mg/1	Tablet, Film coatedOral	Meijer, Inc.	79481-0503
equaline dual action pain relieveracetaminophen, ibuprofen	Acetaminophen 250 mg/1; Ibuprofen 125 mg/1	Tablet, Film coatedOral	United Natural Foods, Inc. dba UNFI	41163-103
equate dual back pain relieveracetaminophen, ibuprofen	Acetaminophen 250 mg/1; Ibuprofen 125 mg/1	Tablet, Film coatedOral	WALMART INC.	79903-326
equate dual pain relieveracetaminophen, ibuprofen	Acetaminophen 250 mg/1; Ibuprofen 125 mg/1	Tablet, Film coatedOral	WALMART INC.	79903-243
equate pain relieveracetaminophen, ibuprofen	Acetaminophen 250 mg/1; Ibuprofen 125 mg/1	Tablet, Film coatedOral	WALMART INC.	79903-148
foster and thrive dual actionacetaminophen, ibuprofen	Acetaminophen 250 mg/1; Ibuprofen 125 mg/1	Tablet, Film coatedOral	Strategic Sourcing Services LLC	70677-1274
good sense dual actionacetaminophen, ibuprofen	Acetaminophen 250 mg/1; Ibuprofen 125 mg/1	Tablet, Film coatedOral	L Perrigo Company	0113-5300
good sense dual actionacetaminophen, ibuprofen	Acetaminophen 250 mg/1; Ibuprofen 125 mg/1	Tablet, Film coatedOral	Sportpharm LLC	85766-044

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Good Sense Dual Action Back Pain (Acetaminophen, ibuprofen) NDC 0113-5299