What is NDC 83324-071?

83324-071 is the product NDC for Childrens Pain and Fever Relief (acetaminophen), Acetaminophen 160 mg/1 tablet, chewable, listed with the FDA by Chain Drug Marketing Association, Inc.. It has 1 package NDC, shown above in 10- and 11-digit form.

What drug is associated with this NDC?

Childrens Pain and Fever Relief (Acetaminophen).

Chain Drug Marketing Association, Inc., NDC labeler code 83324. 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 Pain and Fever Relief?

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 Pain and Fever Relief NDC 83324-071

NDC codes

FDA NDC Directory

Product NDC (as listed)83324-071Labeler and product segments. Claims need a package NDC.

Product NDC at billing width83324-0071Add 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
83324-071-24	83324007124	1 BOTTLE, PLASTIC in 1 CARTON (83324-071-24) / 24 TABLET, CHEWABLE in 1 BOTTLE, PLASTICMarketed from Oct 21, 2024

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 Pain and Fever Relief
Generic name (nonproprietary): acetaminophen
Active ingredients: Acetaminophen — 160 mg/1
Dosage form: Tablet, Chewable
Route: Oral
Labeler: Chain Drug Marketing Association, Inc.NDC labeler code 83324
Product type: Over-the-counter drug
Marketing category: OTC monograph drugApplication M 013
Marketing start: Oct 21, 2024
Listing expires: Dec 31, 2027
Identifiers: Product ID 83324-071_55b17e29-e2b8-480b-88a3-cb7772665806SPL ID 55b17e29-e2b8-480b-88a3-cb7772665806SPL set ID 420a1e05-caa6-481f-bdab-a670f0220f96RxCUI 313820UNII 362O9ITL9DUPC 0635515996021

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

N483324007124 followed by a unit qualifier and the quantity

Package 83324-0071-24. 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 Jun 16, 2026.

Indications (excerpt from the label)

Uses temporarily relieves minor aches and pains due to: headache sore throat flu 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)

About NDC 83324-071

What is NDC 83324-071?: 83324-071 is the product NDC for Childrens Pain and Fever Relief (acetaminophen), Acetaminophen 160 mg/1 tablet, chewable, listed with the FDA by Chain Drug Marketing Association, Inc.. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Childrens Pain and Fever Relief (Acetaminophen).
What is the active ingredient?: Acetaminophen.
Who is the labeler?: Chain Drug Marketing Association, Inc., NDC labeler code 83324. 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 Pain and Fever Relief?: 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 M 013

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

FDA NDC Directory listings under M 013
Product	Strength	Form · route	Labeler	Product NDC
365 whole foods market acetaminophenacetaminophen	Acetaminophen 500 mg/1	TabletOral	Whole Foods Market, INC.	42681-0025
Acetaminophen	Acetaminophen 160 mg/5mL	SolutionOral	PAI Holdings, LLC dba PAI Pharma	0121-0657
Acetaminophen	Acetaminophen 160 mg/5mL	SuspensionOral	PAI Holdings, LLC dba PAI Pharma	0121-0941
Acetaminophen	Acetaminophen 160 mg/5mL	SolutionOral	PAI Holdings, LLC dba PAI Pharma	0121-1047
Acetaminophen	Acetaminophen 325 mg/10.15mL	SolutionOral	PAI Holdings, LLC dba PAI Pharma	0121-1314
Acetaminophen	Acetaminophen 325 mg/10.15mL	SuspensionOral	PAI Holdings, LLC dba PAI Pharma	0121-1882
Acetaminophen	Acetaminophen 650 mg/20.3mL	SolutionOral	PAI Holdings, LLC dba PAI Pharma	0121-1971
Acetaminophen	Acetaminophen 325 mg/10.15mL	SolutionOral	PAI Holdings, LLC dba PAI Pharma	0121-2094
Acetaminophen	Acetaminophen 650 mg/20.3mL	SuspensionOral	PAI Holdings, LLC dba PAI Pharma	0121-2823
Acetaminophen	Acetaminophen 650 mg/20.3mL	SolutionOral	PAI Holdings, LLC dba PAI Pharma	0121-3141
Acetaminophen	Acetaminophen 500 mg/1	TabletOral	WALGREENS	0363-9538
Acetaminophen	Acetaminophen 500 mg/1	TabletOral	WALGREEN CO.	0363-9595
Acetaminophen	Acetaminophen 160 mg/1	TabletOral	WALGREEN CO.	0363-9605
Acetaminophen	Acetaminophen 500 mg/1	TabletOral	WALGREEN CO.	0363-9798
Acetaminophen	Acetaminophen 500 mg/1	TabletOral	Walgreens	0363-9810
Acetaminophen	Acetaminophen 500 mg/1	TabletOral	Rugby Laboratories	0536-1172
Acetaminophen	Acetaminophen 500 mg/1	Tablet, CoatedOral	Rugby Laboratories	0536-1292
Acetaminophen	Acetaminophen 500 mg/1	Tablet, Film coatedOral	Rugby Laboratories	0536-1413
Acetaminophen	Acetaminophen 325 mg/1	Tablet, Film coatedOral	NCS HealthCare of KY, LLC dba Vangard Labs	0615-8608
Acetaminophen	Acetaminophen 325 mg/1	Tablet, Film coatedOral	NCS HealthCare of KY, LLC dba Vangard Labs	0615-8609

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Childrens Pain and Fever Relief (Acetaminophen) NDC 83324-071