What is NDC 67751-219?

67751-219 is the product NDC for Alka-Seltzer Original Flavor, Aspirin 325 mg/1 tablet, effervescent, listed with the FDA by Navajo Manufacturing Company Inc.. It has 2 package NDCs, shown above in 10- and 11-digit form.

Navajo Manufacturing Company Inc., NDC labeler code 67751. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.

What other NDCs exist for Alka-Seltzer Original Flavor?

4 other product NDCs are listed under this name.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

Alka-Seltzer Original Flavor NDC 67751-219

NDC codes

FDA NDC Directory

Product NDC (as listed)67751-219Labeler and product segments. Claims need a package NDC.

Product NDC at billing width67751-0219Add 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
67751-219-01	67751021901	1 POUCH in 1 CARTON (67751-219-01) / 2 TABLET, EFFERVESCENT in 1 POUCHMarketed from Mar 16, 2023
67751-219-02	67751021902	2 POUCH in 1 CARTON (67751-219-02) / 2 TABLET, EFFERVESCENT in 1 POUCHMarketed from Mar 16, 2023

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): Alka-Seltzer Original Flavor
Generic name (nonproprietary): alka-seltzer original flavor
Active ingredients: Aspirin — 325 mg/1
Dosage form: Tablet, Effervescent
Route: Oral
Labeler: Navajo Manufacturing Company Inc.NDC labeler code 67751
Product type: Over-the-counter drug
Marketing category: OTC monograph drugApplication M 013
Marketing start: Mar 16, 2023
Listing expires: Dec 31, 2026
Other FDA classes: Non-Steroidal (Chemical structure)Cyclooxygenase Inhibitors (Mechanism)Decreased Platelet Aggregation (Physiologic effect)Decreased Prostaglandin Production (Physiologic effect)
Identifiers: Product ID 67751-219_23960e84-c184-a473-e063-6394a90ad146SPL ID 23960e84-c184-a473-e063-6394a90ad146SPL set ID f70875ab-241c-4876-e053-6294a90a8092RxCUI 2606079UNII R16CO5Y76E
Pharmacologic class: Nonsteroidal Anti-inflammatory Drug; Platelet Aggregation Inhibitor

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

N467751021901 followed by a unit qualifier and the quantity

Package 67751-0219-01. 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 Oct 3, 2024.

Indications (excerpt from the label)

Uses Uses ● temporarily relieves minor aches and pains due to: ● headache ● muscle pain ● backache ● toothache ● menstrual pain ● colds ● minor pain of arthritis ● temporarily reduces fever

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 67751-219

What is NDC 67751-219?: 67751-219 is the product NDC for Alka-Seltzer Original Flavor, Aspirin 325 mg/1 tablet, effervescent, listed with the FDA by Navajo Manufacturing Company Inc.. It has 2 package NDCs, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Alka-Seltzer Original Flavor.
What is the active ingredient?: Aspirin.
Who is the labeler?: Navajo Manufacturing Company Inc., NDC labeler code 67751. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Alka-Seltzer Original Flavor?: 4 other product NDCs are listed under this name. See all Alka-Seltzer Original Flavor NDCs.
Is there a related HCPCS / J-code?: Not in Med-Code's curated HCPCS directory. See Billing references above.

Other finished products listed under the same name: strengths, forms and labelers.

Other Alka-Seltzer Original Flavor NDCs
Product	Strength	Form · route	Labeler	Product NDC	Package NDCs (11-digit)
Alka-Seltzer Original Flavorbuffered aspirin, effervescent tablet	Aspirin 325 mg/1	Tablet, EffervescentOral	Lil' Drug Store Products, Inc.	66715-9603	66715-9603-0266715-9603-03
Alka-Seltzer Original Flavorbuffered aspirin, effervescent tablet	Aspirin 325 mg/1	Tablet, EffervescentOral	Lil' Drug Store Products, Inc.	66715-6503	66715-6503-02
Alka-Seltzer Original Flavorbuffered aspirin, effervescent tablet	Aspirin 325 mg/1	Tablet, EffervescentOral	Lil' Drug Store Products, Inc.	66715-6403	66715-6403-0266715-6403-0766715-6403-08
Alka-Seltzer Original Flavor	Aspirin 325 mg/1	Tablet, EffervescentOral	Bayer HealthCare LLC.	0280-0087	00280-0087-0100280-0087-0200280-0087-03+2 more

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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