What is NDC 42961-112?

42961-112 is the product NDC for Xpect Cold Relief, Guaifenesin 200 mg/1 + 2 more ingredients tablet, listed with the FDA by Cintas Corporation. It has 2 package NDCs, shown above in 10- and 11-digit form.

What drug is associated with this NDC?

Xpect Cold Relief (Acetaminophen Guaifenesein Phenylephrine HCl).

What is the active ingredient?

Guaifenesin, Acetaminophen, Phenylephrine hydrochloride.

Cintas Corporation, NDC labeler code 42961. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.

What other NDCs exist for Xpect Cold 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.

Xpect Cold Relief NDC 42961-112 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)42961-112Labeler and product segments. Claims need a package NDC.

Product NDC at billing width42961-0112Add 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
42961-112-13	4296101121342961011213	25 PACKET in 1 BAG (42961-112-13) / 2 TABLET in 1 PACKET (42961-112-10)Marketed from Sep 23, 2025
42961-112-14	4296101121442961011214	40 PACKET in 1 BOX (42961-112-14) / 2 TABLET in 1 PACKET (42961-112-10)Marketed from Sep 23, 2025

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): Xpect Cold Relief
Generic name (nonproprietary): acetaminophen guaifenesein phenylephrine hcl
Active ingredients: Guaifenesin — 200 mg/1Acetaminophen — 325 mg/1Phenylephrine hydrochloride — 5 mg/1
Dosage form: Tablet
Route: Oral
Labeler: Cintas CorporationNDC labeler code 42961
Product type: Over-the-counter drug
Marketing category: OTC monograph drugApplication M 013
Marketing start: Mar 29, 2021
Listing expires: Dec 31, 2027
Other FDA classes: Adrenergic alpha1-Agonists (Mechanism)Decreased Respiratory Secretion Viscosity (Physiologic effect)Increased Respiratory Secretions (Physiologic effect)
Identifiers: Product ID 42961-112_59bbb82a-0247-417c-b0ed-991646373be8SPL ID 59bbb82a-0247-417c-b0ed-991646373be8SPL set ID 02391d55-32b2-4083-9315-98e9b3650c55RxCUI 1243679UNII 495W7451VQ, 362O9ITL9D, 04JA59TNSJ
Pharmacologic class: Expectorant; 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

N442961011213 followed by a unit qualifier and the quantity

Package 42961-0112-13. 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 Jan 8, 2026.

Indications (excerpt from the label)

Uses temporarily relieves these symptoms associated with hay fever or other respiratory allergies, and the common cold: headache, nasal congestion, minor aches and pains, sinus congestion and pressure helps loosen phlegm (mucus) and thin bronchial secretions to make coughs more productive temporarily reduces fever

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 42961-112

What is NDC 42961-112?: 42961-112 is the product NDC for Xpect Cold Relief, Guaifenesin 200 mg/1 + 2 more ingredients tablet, listed with the FDA by Cintas Corporation. It has 2 package NDCs, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Xpect Cold Relief (Acetaminophen Guaifenesein Phenylephrine HCl).
What is the active ingredient?: Guaifenesin, Acetaminophen, Phenylephrine hydrochloride.
Who is the labeler?: Cintas Corporation, NDC labeler code 42961. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Xpect Cold 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
Childrens Acetaminophenacetaminophen	Acetaminophen 160 mg/5mL	SuspensionOral	Grocery Outlet, Inc.	85828-922
Pain Relief Regular Strengthacetaminophen	Acetaminophen 325 mg/1	TabletOral	CHAIN DRUG MARKETING ASSOCIATION INC	83324-076
equate pain and fever childrensacetaminophen	Acetaminophen 160 mg/5mL	SuspensionOral	Wal-Mart Stores Inc	49035-042
good neighbor pharmacy childrens pain and feveracetaminophen	Acetaminophen 160 mg/5mL	SuspensionOral	Amerisource Bergen	46122-210
Aspirin	Aspirin 81 mg/1	Tablet, Delayed releaseOral	GOODSENSE	50804-880
Tylenol PM Extra Strengthacetaminophen and diphenhydramine hydrochloride	Acetaminophen 500 mg/1; Diphenhydramine hydrochloride 25 mg/1	Tablet, Film coatedOral	Morning Star OTC	53209-1002
Acetaminophen	Acetaminophen 500 mg/1	TabletOral	Cardinal Health 107, LLC	55154-7897
Headache Formula Extra Strengthacetaminophen, aspirin, caffeine	Acetaminophen 250 mg/1 + 2 more ingredients	Tablet, Film coatedOral	ARMY AND AIR FORCE EXCHANGE SERVICE	55301-334
childrens pain and feveracetaminophen	Acetaminophen 160 mg/5mL	SuspensionOral	Walgreen Company	0363-1239
Tylenol PMacetaminophen, diphenhydramine hydrochloride	Acetaminophen 500 mg/1; Diphenhydramine hydrochloride 25 mg/1	Tablet, Film coatedOral	Savings Distributors LLC	73097-013
Alka-Seltzer Originalanhydrous citric acid, aspirin, and sodium bicarbonate	Anhydrous citric acid 1000 mg/1 + 2 more ingredients	Tablet, EffervescentOral	Bayer HealthCare LLC.	0280-4000
Aspirin Low Doseaspirin	Aspirin 81 mg/1	Tablet, Delayed releaseOral	Strategic Sourcing Services LLC	70677-1260
basic care infants pain and feveracetaminophen	Acetaminophen 160 mg/5mL	SuspensionOral	Amazon.com Services LLC	72288-946
Acetaminophen	Acetaminophen 500 mg/1	TabletOral	Sportpharm LLC	85766-223
Pain Relief Aspirin Low Doseaspirin	Aspirin 81 mg/1	Tablet, Delayed releaseOral	Rite Aid Corporation	11822-0600
Equaline Effervescent Antacid and Pain Reliefaspirin, citric acid, sodium bicarbonate	Aspirin 325 mg/1 + 2 more ingredients	Tablet, EffervescentOral	United Natural Foods, Inc. dba UNFI	41163-421
Night Time Severe Cold and Cough Reliefacetaminophen, diphenhydramine hcl, phenylephrine hcl	Acetaminophen 325 mg/15mL + 2 more ingredients	LiquidOral	Chain Drug Consortium, LLC	68016-154
Tension Headache Relief	Acetaminophen 500 mg/1; Caffeine 65 mg/1	Capsule, CoatedOral	Allegiant Health	69168-001
Childrens Acetaminophenacetaminophen	Acetaminophen 160 mg/5mL	SuspensionOral	Proficient Rx LP	71205-263
Chewable Aspirinaspirin	Aspirin 81 mg/1	Tablet, ChewableOral	Chain Drug Marketing Association, Inc.	83324-075

Showing 20 of 40.