What is NDC 69197-029?

69197-029 is the product NDC for Sed-Max (acetaminophen 500 mg with caffeine 65mg), Acetaminophen 500 mg/1; Caffeine 65 mg/1 tablet, coated, listed with the FDA by Command Brands, LLC. It has 1 package NDC, shown above in 10- and 11-digit form.

What drug is associated with this NDC?

Sed-Max (Acetaminophen 500 mg with Caffeine 65mg).

Command Brands, LLC, NDC labeler code 69197. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.

What other NDCs exist for Sed-Max?

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.

Sed-Max NDC 69197-029 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)69197-029Labeler and product segments. Claims need a package NDC.

Product NDC at billing width69197-0029Add 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
69197-029-20	69197002920	1 BOTTLE in 1 CARTON (69197-029-20) / 20 TABLET, COATED in 1 BOTTLEMarketed from Nov 26, 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): Sed-Max
Generic name (nonproprietary): acetaminophen 500 mg with caffeine 65mg
Active ingredients: Acetaminophen — 500 mg/1Caffeine — 65 mg/1
Dosage form: Tablet, Coated
Route: Oral
Labeler: Command Brands, LLCNDC labeler code 69197
Product type: Over-the-counter drug
Marketing category: OTC monograph drugApplication M 013
Marketing start: Nov 26, 2014
Listing expires: Dec 31, 2026
Other FDA classes: Central Nervous System Stimulation (Physiologic effect)Xanthines (Chemical structure)
Identifiers: Product ID 69197-029_bd14fe1d-1a3f-4854-aab9-dbcd09046365SPL ID bd14fe1d-1a3f-4854-aab9-dbcd09046365SPL set ID 4920a0e9-6f88-4df0-8657-77c95a3b9617RxCUI 307686, 1866143UNII 362O9ITL9D, 3G6A5W338E
Pharmacologic class: Central Nervous System Stimulant; Methylxanthine

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

N469197002920 followed by a unit qualifier and the quantity

Package 69197-0029-20. 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 19, 2017.

Indications (excerpt from the label)

Uses temporary relief of minor aches and pains due to: ■ headache ■ muscular aches

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 69197-029

What is NDC 69197-029?: 69197-029 is the product NDC for Sed-Max (acetaminophen 500 mg with caffeine 65mg), Acetaminophen 500 mg/1; Caffeine 65 mg/1 tablet, coated, listed with the FDA by Command Brands, LLC. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Sed-Max (Acetaminophen 500 mg with Caffeine 65mg).
What is the active ingredient?: Acetaminophen, Caffeine.
Who is the labeler?: Command Brands, LLC, NDC labeler code 69197. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Sed-Max?: 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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Sed-Max (Acetaminophen 500 mg with caffeine 65mg) NDC 69197-029