What is NDC 63868-747?

63868-747 is the product NDC for Pressure Pain Mucus PE, Acetaminophen 325 mg/1 + 2 more ingredients tablet, coated, listed with the FDA by Chain Drug Marketing Association. It has 1 package NDC, shown above in 10- and 11-digit form.

What drug is associated with this NDC?

Pressure Pain Mucus PE (ACETAMINOPHEN, GUAIFENESIN, and PHENYLEPHRINE HYDROCHLORIDE).

What is the active ingredient?

Acetaminophen, Guaifenesin, Phenylephrine hydrochloride.

Chain Drug Marketing Association, NDC labeler code 63868. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.

What other NDCs exist for Pressure Pain Mucus PE?

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.

Pressure Pain Mucus PE NDC 63868-747

NDC codes

FDA NDC Directory

Product NDC (as listed)63868-747Labeler and product segments. Claims need a package NDC.

Product NDC at billing width63868-0747Add 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
63868-747-24	6386807472463868074724	2 BLISTER PACK in 1 CARTON (63868-747-24) / 12 TABLET, COATED in 1 BLISTER PACKMarketed from May 21, 2014

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): Pressure Pain Mucus PE
Generic name (nonproprietary): acetaminophen, guaifenesin, and phenylephrine hydrochloride
Active ingredients: Acetaminophen — 325 mg/1Guaifenesin — 200 mg/1Phenylephrine hydrochloride — 5 mg/1
Dosage form: Tablet, Coated
Route: Oral
Labeler: Chain Drug Marketing AssociationNDC labeler code 63868
Product type: Over-the-counter drug
Marketing category: OTC monograph (final)Application part341
Marketing start: May 21, 2014
Listing expires: Dec 31, 2026
Other FDA classes: Adrenergic alpha1-Agonists (Mechanism)
Identifiers: Product ID 63868-747_7e555b65-5cdd-2eb5-e053-2991aa0a8dceSPL ID 7e555b65-5cdd-2eb5-e053-2991aa0a8dceSPL set ID 1e54ecb3-c3c3-477a-8725-23f24e77a44bRxCUI 1243679UNII 362O9ITL9D, 495W7451VQ, 04JA59TNSJUPC 0635515987395
Pharmacologic class: 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

N463868074724 followed by a unit qualifier and the quantity

Package 63868-0747-24. 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 Dec 31, 2018.

Indications (excerpt from the label)

Uses temporarily relieves these symptoms associated with hay fever or other upper respiratory allergies, and the common cold: sinus congestion and pressure headache minor aches and pains nasal congestion helps loosen phlegm (mucus) and thin bronchial secretions to rid the bronchial passageways of bothersome mucus and 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 63868-747

What is NDC 63868-747?: 63868-747 is the product NDC for Pressure Pain Mucus PE, Acetaminophen 325 mg/1 + 2 more ingredients tablet, coated, listed with the FDA by Chain Drug Marketing Association. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Pressure Pain Mucus PE (ACETAMINOPHEN, GUAIFENESIN, and PHENYLEPHRINE HYDROCHLORIDE).
What is the active ingredient?: Acetaminophen, Guaifenesin, Phenylephrine hydrochloride.
Who is the labeler?: Chain Drug Marketing Association, NDC labeler code 63868. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Pressure Pain Mucus PE?: 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
Pseudo Time PEphenylephrine hchloride	Phenylephrine hydrochloride 10 mg/1	Tablet, Film coatedOral	TIME CAP LABORATORIES, INC.	49483-234
Allergy Timechlorpheniramine maleate	Chlorpheniramine maleate 4 mg/1	TabletOral	Time Cap Labs Inc	49483-242
Diphenhydramine Hydrochloride	Diphenhydramine hydrochloride 25 mg/1	Tablet, CoatedOral	Time-Cap Labs, Inc	49483-329
CVS Health Sinus Reliefoxymetazoline hydrochloride	Oxymetazoline hydrochloride .0005 g/mL	SprayNasal	CVS Pharmacy,Inc.	59779-787
Severe Cold Head Congestionacetaminophen, guaifenesin, and phenylephrine hydrochloride	Acetaminophen 325 mg/1 + 2 more ingredients	Tablet, CoatedOral	Marc Glassman, Inc.	68998-175
CVS Health Childrens Allergy Reliefdiphenhydramine hydrochloride	Diphenhydramine hydrochloride 12.5 mg/5mL	LiquidOral	CVS Pharmacy,Inc.	59779-793
CVS Health Four Actions Nasal Decongestantphenylephrine hydrochloride	Phenylephrine hydrochloride 10 mg/mL	SprayNasal	CVS Pharmacy,Inc.	59779-838
Tussin CFdextromethorphan hbr guaifenesin phenylephrine hcl	Dextromethorphan hydrobromide 20 mg/10mL + 2 more ingredients	SolutionOral	Strategic Sourcing Services	70677-1187
Tussinguaifenesin	Guaifenesin 200 mg/10mL	SolutionOral	Strategic Sourcing Services	70677-1186
Discount Drug Mart Value Vapor Steamcamphor (synthetic)	Camphor (Synthetic) .623 g/10mL	LiquidRespiratory (Inhalation)	Drug Mart	53943-256
NightTime Cold and Fluacetaminophen,dextromethorphan,doxylamine	Acetaminophen 325 mg/1 + 2 more ingredients	Capsule, Liquid filledOral	Velocity Pharma	76168-056
Allergydiphenhydramine hydrochloride	Diphenhydramine hydrochloride 25 mg/1	TabletOral	Velocity Pharma LLC	76168-121
Nightime Sleep Aiddiphenhydramine	Diphenhydramine hydrochloride 50 mg/1	Capsule, Liquid filledOral	Velocity Pharma	76168-065
Diphenhydramine Hydrochloride	Diphenhydramine hydrochloride 25 mg/1	CapsuleOral	Epic Pharma, LLC	42806-648
Diphenhydramine Hydrochloride	Diphenhydramine hydrochloride 50 mg/1	CapsuleOral	Epic Pharma, LLC	42806-649
Pi Yuan Chinnaphazoline hydrochloride	Naphazoline hydrochloride 1 mg/1	Solution/ dropsNasal	International Nature Nutraceuticals	51367-035
Sugar Free Cherry Cough Dropsmenthol	Menthol 5.8 1/1	LozengeOral	Army & Air Force Exchange Service	55301-038
Walgreens Adult Nighttime Wal Tussin DM Max Maximum Strengthdextromethorphan hbr, doxylamine succinate	Dextromethorphan hydrobromide 30 mg/20mL; Doxylamine succinate 12.5 mg/20mL	SolutionOral	WALGREEN CO.	0363-0758
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

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