What is NDC 83324-023?

83324-023 is the product NDC for QCH Adult Tussin DM 542, Dextromethorphan hydrobromide 20 mg/20mL; Guaifenesin 200 mg/20mL liquid, listed with the FDA by Chain Drug Marketing Association Inc.. It has 2 package NDCs, shown above in 10- and 11-digit form.

What drug is associated with this NDC?

QCH Adult Tussin DM 542 (Dextromethorphan HBr, Guaifenesin).

What is the active ingredient?

Dextromethorphan hydrobromide, Guaifenesin.

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 QCH Adult Tussin DM 542?

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.

QCH Adult Tussin DM 542 NDC 83324-023

NDC codes

FDA NDC Directory

Product NDC (as listed)83324-023Labeler and product segments. Claims need a package NDC.

Product NDC at billing width83324-0023Add 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
83324-023-04	8332400230483324002304	1 BOTTLE in 1 CARTON (83324-023-04) / 118 mL in 1 BOTTLEMarketed from May 8, 2024
83324-023-08	8332400230883324002308	1 BOTTLE in 1 CARTON (83324-023-08) / 237 mL in 1 BOTTLEMarketed from May 8, 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): QCH Adult Tussin DM 542
Generic name (nonproprietary): dextromethorphan hbr, guaifenesin
Active ingredients: Dextromethorphan hydrobromide — 20 mg/20mLGuaifenesin — 200 mg/20mL
Dosage form: Liquid
Route: Oral
Labeler: Chain Drug Marketing Association Inc.NDC labeler code 83324
Product type: Over-the-counter drug
Marketing category: OTC monograph drugApplication part341
Marketing start: May 8, 2024
Listing expires: Dec 31, 2026
Other FDA classes: Decreased Respiratory Secretion Viscosity (Physiologic effect)Increased Respiratory Secretions (Physiologic effect)Sigma-1 Receptor Agonists (Mechanism)Uncompetitive NMDA Receptor Antagonists (Mechanism)
Identifiers: Product ID 83324-023_41a95b6d-6e0a-4729-ac06-3963a78a0e51SPL ID 41a95b6d-6e0a-4729-ac06-3963a78a0e51SPL set ID 17caffa4-a264-7f3e-e063-6394a90ac419RxCUI 1790650UNII 9D2RTI9KYH, 495W7451VQ
Pharmacologic class: Expectorant; Sigma-1 Agonist; Uncompetitive N-methyl-D-aspartate Receptor Antagonist

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

N483324002304 followed by a unit qualifier and the quantity

Package 83324-0023-04. 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 May 8, 2024.

Indications (excerpt from the label)

USE(S) temporarily relieves cough due too minor throat and bronchial irritation as may occur with a cold helps loosen phlegm (mucus) and thin bronchial secretions to drain bronchial tubes

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 83324-023

What is NDC 83324-023?: 83324-023 is the product NDC for QCH Adult Tussin DM 542, Dextromethorphan hydrobromide 20 mg/20mL; Guaifenesin 200 mg/20mL liquid, listed with the FDA by Chain Drug Marketing Association Inc.. It has 2 package NDCs, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: QCH Adult Tussin DM 542 (Dextromethorphan HBr, Guaifenesin).
What is the active ingredient?: Dextromethorphan hydrobromide, Guaifenesin.
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 QCH Adult Tussin DM 542?: 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 part341

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

FDA NDC Directory listings under part341
Product	Strength	Form · route	Labeler	Product NDC
Broncochem Kids Allergy Controlchlorpheniramine maleate-dextromethrophan hbr	Chlorpheniramine maleate 2 mg/10mL; Dextromethorphan hydrobromide 10 mg/10mL	SyrupOral	LABORATORIO MAGANCEHM INTERNATIONAL SRL	65131-418
Weeks and Leo Medicated Vaporizing Steamcamphor (synthetic)	Camphor (Synthetic) .623 g/10mL	LiquidRespiratory (Inhalation)	Weeks & Leo Co., Inc.	11383-256
Best Choice Effervescent Cold Reliefaspirin, chlorpheniramine maleate, phenylephrine bitartrate	Aspirin 325 mg/1 + 2 more ingredients	Tablet, EffervescentOral	Valu Merchandiser Company	63941-873
CVS Health Nighttime Sleep Aiddiphenhydramine hydrochloride	Diphenhydramine hydrochloride 50 mg/30mL	LiquidOral	CVS Pharmacy,Inc.	69842-753
Broncochem Maximum Coughdextromethorphan hbr-gyaifenesin	Dextromethorphan hydrobromide 30 mg/10mL; Guaifenesin 200 mg/10mL	SyrupOral	LABORATORIO MAGNACHEM INTERNATIONAL SRL	65131-091
Assured Vaporizing Chest Rubcamphor and eucalyptus oil and menthol	Camphor (Synthetic) 4.7 g/100g + 2 more ingredients	OintmentTopical	Greenbrier International, Inc.	33992-7991
Assured Vaporizing Chest Rubcamphor and eucalyptus oil and menthol	Camphor (Synthetic) 4.7 g/100g + 2 more ingredients	OintmentTopical	Greenbrier International, Inc.	33992-7992
Broncochem Kids Cold And Fluacetaminophen-phenylephrine hcl-guaifenesin	Acetaminophen 325 mg/10mL + 2 more ingredients	SyrupOral	LABORATORIO MAGNACHEM INTERNATIONAL SRL	65131-054
Broncochem Allergy Controlcholpheniramine maleate-phenylephrine hcl	Chlorpheniramine maleate 4 mg/10mL; Phenylephrine hydrochloride 10 mg/10mL	SyrupOral	LABORATORIO MAGNACHEM INTERNATIONAL SRL	65131-098
Diphenhydramine Hydrochloride	Diphenhydramine hydrochloride 50 mg/1	TabletOral	Advance Pharmaceutical Inc.	17714-023
Diphenhydramine Hydrochloride	Diphenhydramine hydrochloride 25 mg/1	CapsuleOral	Advance Pharmaceutical Inc.	17714-020
Diphenhydramine Hydrochloride	Diphenhydramine hydrochloride 50 mg/1	CapsuleOral	Advance Pharmaceutical Inc.	17714-021
Diphenhydramine Hydrochloride	Diphenhydramine hydrochloride 25 mg/1	TabletOral	Advance Pharmaceutical Inc.	17714-135
Childrens Multi-symptom Cold Daytimedextromethorphan hbr, guaifenesin, phenylephrine hcl	Dextromethorphan hydrobromide 5 mg/5mL + 2 more ingredients	LiquidOral	Wal-Mart Stores, Inc.	79903-270
Effervescent Cold Reliefaspirin, chlorpheniramine maleate, phenylephrine bitartrate	Aspirin 325 mg/1 + 2 more ingredients	Tablet, EffervescentOral	Discount Drug Mart	53943-873
Acetaminophen PM	Acetaminophen 500 mg/1; Diphenhydramine hydrochloride 25 mg/1	TabletOral	Advance Pharmaceutical Inc.	17714-133
Mucus Relief Cough and Congestion DMguaifenesin and dextromethorphan hbr	Dextromethorphan hydrobromide 20 mg/1; Guaifenesin 400 mg/1	TabletOral	Advance Pharmaceutical Inc.	17714-150
Childrens Multi-symptom Cold and Fever Liquidacetaminophen, dextromethorphan hbr, guaifenesin, phenylephrine hcl	Acetaminophen 325 mg/10mL + 3 more ingredients	LiquidOral	Wal-Mart Stores, Inc.	49035-772
Mucus Reliefguaifenesin 400 mg	Guaifenesin 400 mg/1	TabletOral	Advance Pharmaceutical Inc.	17714-152
Childrens Mucus and Cough Reliefdextromethorphan hbr, guaifenesin	Dextromethorphan hydrobromide 5 mg/5mL; Guaifenesin 100 mg/5mL	LiquidOral	Family Dollar Services, Inc.	55319-924

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QCH Adult Tussin DM 542 (Dextromethorphan hbr, guaifenesin) NDC 83324-023