What is NDC 69842-314?

69842-314 is the product NDC for CVS Antibacterial Plus Urinary Pain Relief, Methenamine 162 mg/1; Sodium salicylate 162.5 mg/1 tablet, listed with the FDA by CVS Pharmacy, Inc. It has 1 package NDC, shown above in 10- and 11-digit form.

What drug is associated with this NDC?

CVS Antibacterial Plus Urinary Pain Relief (Methenamine, Sodium salicylate).

What is the active ingredient?

Methenamine, Sodium salicylate.

CVS Pharmacy, Inc, NDC labeler code 69842. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.

What other NDCs exist for CVS Antibacterial Plus Urinary Pain 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.

NDC 69842-314

NDC codes

FDA NDC Directory

Product NDC (as listed)69842-314Labeler and product segments. Claims need a package NDC.

Product NDC at billing width69842-0314Add 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
69842-314-24	6984203142469842031424	1 BLISTER PACK in 1 CARTON (69842-314-24) / 24 TABLET in 1 BLISTER PACKMarketed from Feb 22, 2017

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): CVS Antibacterial Plus Urinary Pain Relief
Generic name (nonproprietary): methenamine, sodium salicylate
Active ingredients: Methenamine — 162 mg/1Sodium salicylate — 162.5 mg/1
Dosage form: Tablet
Route: Oral
Labeler: CVS Pharmacy, IncNDC labeler code 69842
Product type: Over-the-counter drug
Marketing category: Unapproved drug (other)
Marketing start: Feb 22, 2017
Listing expires: Dec 31, 2026
Identifiers: Product ID 69842-314_23d0e090-48f8-4516-9d16-b6a75d0da31bSPL ID 23d0e090-48f8-4516-9d16-b6a75d0da31bSPL set ID 46384be0-e4b2-4a1e-81b8-6945d5ad7ed2RxCUI 1489932UNII J50OIX95QV, WIQ1H85SYP

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

N469842031424 followed by a unit qualifier and the quantity

Package 69842-0314-24. 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 18, 2024.

Indications (excerpt from the label)

Uses Temporarily relieves: pain & burning • frequency and urgency of urination

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 69842-314

What is NDC 69842-314?: 69842-314 is the product NDC for CVS Antibacterial Plus Urinary Pain Relief, Methenamine 162 mg/1; Sodium salicylate 162.5 mg/1 tablet, listed with the FDA by CVS Pharmacy, Inc. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: CVS Antibacterial Plus Urinary Pain Relief (Methenamine, Sodium salicylate).
What is the active ingredient?: Methenamine, Sodium salicylate.
Who is the labeler?: CVS Pharmacy, Inc, NDC labeler code 69842. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for CVS Antibacterial Plus Urinary Pain 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.

CVS Antibacterial Plus Urinary Pain Relief (Methenamine, sodium salicylate) NDC 69842-314