What is NDC 69842-346?

69842-346 is the product NDC for Bismuth Subsalicylate, Bismuth subsalicylate 262 mg/1 tablet, film coated, listed with the FDA by CVS Pharmacy, Inc.. It has 2 package NDCs, shown above in 10- and 11-digit form.

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 Bismuth Subsalicylate?

2 other product NDCs are listed under this name.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

Bismuth Subsalicylate NDC 69842-346

NDC codes

FDA NDC Directory

Product NDC (as listed)69842-346Labeler and product segments. Claims need a package NDC.

Product NDC at billing width69842-0346Add 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
69842-346-12	6984203461269842034612	1 BOTTLE in 1 CARTON (69842-346-12) / 24 TABLET, FILM COATED in 1 BOTTLEMarketed from Jul 6, 2018
69842-346-28	6984203462869842034628	1 BOTTLE in 1 CARTON (69842-346-28) / 40 TABLET, FILM COATED in 1 BOTTLEMarketed from Jul 6, 2018

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): Bismuth Subsalicylate
Generic name (nonproprietary): bismuth subsalicylate
Active ingredients: Bismuth subsalicylate — 262 mg/1
Dosage form: Tablet, Film coated
Route: Oral
Labeler: CVS Pharmacy, Inc.NDC labeler code 69842
Product type: Over-the-counter drug
Marketing category: OTC monograph drugApplication M 001
Marketing start: Jul 6, 2018
Listing expires: Dec 31, 2027
Identifiers: Product ID 69842-346_4b96475f-d966-11d4-e063-6394a90a0361SPL ID 4b96475f-d966-11d4-e063-6394a90a0361SPL set ID 6dd7c01c-5726-e6db-e053-2a91aa0a968dRxCUI 308760UNII 62TEY51RR1UPC 0050428002391

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

N469842034612 followed by a unit qualifier and the quantity

Package 69842-0346-12. 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 Feb 24, 2026.

Indications (excerpt from the label)

Uses relieves: ■ travelers’ diarrhea ■ diarrhea ■ upset stomach due to overindulgence in food and drink, including: ■ heartburn ■ indigestion ■ nausea ■ gas ■ belching ■ fullness

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 69842-346

What is NDC 69842-346?: 69842-346 is the product NDC for Bismuth Subsalicylate, Bismuth subsalicylate 262 mg/1 tablet, film coated, listed with the FDA by CVS Pharmacy, Inc.. It has 2 package NDCs, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Bismuth Subsalicylate.
What is the active ingredient?: Bismuth subsalicylate.
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 Bismuth Subsalicylate?: 2 other product NDCs are listed under this name. See all Bismuth Subsalicylate 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 Bismuth Subsalicylate NDCs
Product	Strength	Form · route	Labeler	Product NDC	Package NDCs (11-digit)
Bismuth subsalicylate	Bismuth subsalicylate 262 mg/1	Capsule, Liquid filledOral	Softgel Healthcare Pvt Ltd	35916-0234	35916-0234-01
Bismuth Subsalicylate	Bismuth subsalicylate 262 mg/1	Tablet, Film coatedOral	LEADER/ Cardinal Health 110, Inc.	70000-0594	70000-0594-01

Other NDCs under M 001

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

FDA NDC Directory listings under M 001
Product	Strength	Form · route	Labeler	Product NDC
Soothe Chewablecitric acid	Citric acid monohydrate 1.5 g/108.27g	Chewable gelOral	Carolina Cannabis Creations LLC	82876-840
ultra strength antacidantacid	Calcium carbonate 1000 mg/1	Tablet, ChewableOral	Target Corporation	11673-933
Rolaids Extra Strength Mintcalcium carbonate and magnesium hydroxide	Calcium carbonate 675 mg/1; Magnesium hydroxide 135 mg/1	Tablet, ChewableOral	Chattem, Inc.	41167-1001
Extra Strength Antacidcalcium carbonate	Calcium carbonate 750 mg/1	Tablet, ChewableOral	Grocery Outlet, Inc.	85828-903
Medique Alcalakcalcium carbonate	Calcium carbonate 420 mg/1	Tablet, ChewableOral	Unifirst First Aid Corporation	47682-201
Ultra Strength Antacidcalcium carbonate	Calcium carbonate 1000 mg/1	Tablet, ChewableOral	CVS	51316-171
Kirkland Ultra Stregth Antacid 171ABcalcium carbonate	Calcium carbonate 1000 mg/1	TabletOral	COSTCO WHOLESALE COMPANY	63981-171
Regular Strength Antacidcalcium carbonate	Calcium carbonate 500 mg/1	Tablet, ChewableOral	Harris Teeter, LLC	69256-138
Ultra Strength Antacidcalcium carbonate	Calcium carbonate 1000 mg/1	Tablet, ChewableOral	Grocery Outlet, Inc.	85828-905
Magnesium Oxide	Magnesium oxide 400 mg/1	TabletOral	A-S Medication Solutions	50090-7432
Ultra Strength Assorted Berry Antacidcalcium carbonate	Calcium carbonate 1000 mg/1	Tablet, ChewableOral	Harris Teeter, LLC	69256-171
Antacid- Calcium Carbonatecalcium carbonate	Calcium carbonate 1000 mg/1	Tablet, ChewableOral	Anhui Jiuhe Health Industry Co., Ltd	87745-001
Tums Chewy Bitescalcium carbonate	Calcium carbonate 1000 mg/1	Tablet, ChewableOral	Haleon US Holdings LLC	0135-0183
De La Cruz Desempachosodium bicarbonate	Sodium bicarbonate 525 mg/15mL	LiquidOral	DLC LABORATORIES, INC.	24286-1523
HEB Wild Berry Antacid Chewscalcium carbonate	Calcium carbonate 750 mg/1	Tablet, ChewableOral	HEB	37808-493
Unishield Antacidcalcium carbonate	Calcium carbonate 420 mg/1	Tablet, ChewableOral	Unishield	49314-1013
Calmicid AC Acid Reducerfamotidine	Famotidine 20 mg/1	Tablet, CoatedOral	Melaleuca, Inc.	54473-411
Exchange Select Antacid Tropical Fruitcalcium carbonate	Calcium carbonate 750 mg/1	Tablet, ChewableOral	ARMY AND AIR FORCE EXCHANGE SERVICE	55301-102
Leader Extra Strength Sugar Free Antacidantacid	Calcium carbonate 750 mg/1	Tablet, ChewableOral	Cardinal Health	70000-0460
Sodium Bicarbonate Antacidsodium bicarbonate	Sodium bicarbonate 650 mg/1	TabletOral	Aphena Pharma Solutions - Tennessee, LLC	71610-669

Showing 20 of 40.