Stomach

Product NDC: 66715-6855
11-digit product format: 667156855
Labeler code: 66715
Product ID: 66715-6855_17cb55a2-da1f-8ada-e063-6394a90a63e1
Type: HUMAN OTC DRUG
Nonproprietary name: Bismuth Subsalicylate
Dosage form: LIQUID
Route: ORAL
Labeler: Lil' Drug Store Products, Inc
Application: M001
Marketing category: OTC MONOGRAPH DRUG
Marketing start: 2014-12-01
Substance: BISMUTH SUBSALICYLATE
Active strength: 525 mg/30mL
Pharmacologic classes: Bismuth [CS], Bismuth [EPC]
NDC exclude flag: No
Listing certified through: 2026-12-31
Current FDA listing: Yes

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.

Additional Listing Data#

Finished product: Yes
Brand name base: Stomach
Brand name suffix: Lil Drug Store Products
Listing expiration: 2026-12-31

Active Ingredients#

Ingredient, Strength table
Ingredient	Strength
BISMUTH SUBSALICYLATE	525 mg/30mL

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
62TEY51RR1	Internal UNII lookup

Harmonized RxCUI identifiers#

RxCUI identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
308762	Internal RxNorm lookup

Harmonized SPL set identifiers#

SPL set identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
05e14009-b35d-4711-b6f0-89b6d060b387	Available on FDA.report

DailyMed Product Concepts#

Product concept, Relation, Version table
Product concept	Relation	Version	Effective
0be8e4ae-4d57-49f3-b3a9-e4728b4e8d15	Product name	1	20240313
c6f86816-7da6-43ea-8c25-ac9758311cc5	Product name	1	20220118
3c386306-c48a-413e-bb69-70cb268496f3	Product name	1	20210727
dea2eded-d1e7-46bb-9a3d-f8dc20de6277	Product name	1	20190408
252e11b6-1a9a-4283-a242-df2c129c496d	Product name	3	20170717

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
66715-6855-4	StomachLil Drug Store Products	237 mL in 1 BOTTLE, PLASTIC	LIQUID	237		7

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	DailyMed label	SPL version
Bismuth Subsalicylate	ACTIVE INGREDIENT	62TEY51RR1	STOMACH LIL DRUG STORE PRODUCTS (BISMUTH SUBSALICYLATE) LIQUID [LIL' DRUG STORE PRODUCTS, INC]	1
Bismuth Cation	ACTIVE MOIETY	ZS9CD1I8YE	STOMACH LIL DRUG STORE PRODUCTS (BISMUTH SUBSALICYLATE) LIQUID [LIL' DRUG STORE PRODUCTS, INC]	1
Benzoic acid	INACTIVE INGREDIENT	8SKN0B0MIM	STOMACH LIL DRUG STORE PRODUCTS (BISMUTH SUBSALICYLATE) LIQUID [LIL' DRUG STORE PRODUCTS, INC]	1
D&C red NO. 22	INACTIVE INGREDIENT	1678RKX8RT	STOMACH LIL DRUG STORE PRODUCTS (BISMUTH SUBSALICYLATE) LIQUID [LIL' DRUG STORE PRODUCTS, INC]	1
D&C red NO. 28	INACTIVE INGREDIENT	767IP0Y5NH	STOMACH LIL DRUG STORE PRODUCTS (BISMUTH SUBSALICYLATE) LIQUID [LIL' DRUG STORE PRODUCTS, INC]	1
Magnesium aluminum silicate	INACTIVE INGREDIENT	6M3P64V0NC	STOMACH LIL DRUG STORE PRODUCTS (BISMUTH SUBSALICYLATE) LIQUID [LIL' DRUG STORE PRODUCTS, INC]	1
Saccharin sodium	INACTIVE INGREDIENT	SB8ZUX40TY	STOMACH LIL DRUG STORE PRODUCTS (BISMUTH SUBSALICYLATE) LIQUID [LIL' DRUG STORE PRODUCTS, INC]	1
salicylic acid	INACTIVE INGREDIENT	O414PZ4LPZ	STOMACH LIL DRUG STORE PRODUCTS (BISMUTH SUBSALICYLATE) LIQUID [LIL' DRUG STORE PRODUCTS, INC]	1
sodium salicylate	INACTIVE INGREDIENT	WIQ1H85SYP	STOMACH LIL DRUG STORE PRODUCTS (BISMUTH SUBSALICYLATE) LIQUID [LIL' DRUG STORE PRODUCTS, INC]	1
sorbic acid	INACTIVE INGREDIENT	X045WJ989B	STOMACH LIL DRUG STORE PRODUCTS (BISMUTH SUBSALICYLATE) LIQUID [LIL' DRUG STORE PRODUCTS, INC]	1
Water	INACTIVE INGREDIENT	059QF0KO0R	STOMACH LIL DRUG STORE PRODUCTS (BISMUTH SUBSALICYLATE) LIQUID [LIL' DRUG STORE PRODUCTS, INC]	1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
66715-6855	STOMACH LIL DRUG STORE PRODUCTS (BISMUTH SUBSALICYLATE) LIQUID STOMACH CIRCLE K (BISMUTH SUBSALICYLATE) LIQUID [LIL' DRUG STORE PRODUCTS, INC]	7	Current NDC, Legacy NDC, 1 package rows	20240507_05e14009-b35d-4711-b6f0-89b6d060b387.zip

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 2 of 36 · 719 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Kroger Extra Strength Sugar Free	CALCIUM CARBONATE	KROGER COMPANY	3f737ce2-961e-4bd0-ae6d-078248cf1c67	2026-08-31	Warnings	Exact identifier application number: M001
Kroger Extra Strength Assorted Berry	CALCIUM CARBONATE	KROGER COMPANY	fa191237-d230-4528-8dff-50e8d5c65b6d	2026-08-31	Warnings	Exact identifier application number: M001
Kroger Ultra Strength Assorted Berry	CALCIUM CARBONATE	KROGER COMPANY	b7db77a7-0580-455b-a2ef-a68584f03981	2026-08-31	Warnings	Exact identifier application number: M001
Ultra Strength Natural Antacid	CALCIUM CARBONATE	KROGER COMPANY	2931d427-b2be-4db9-a58d-ff89c221ff51	2026-08-31	Warnings	Exact identifier application number: M001
Ultra Strength Antacid	ANTACID TABLETS	THE KROGER CO.,	f5d82d1b-2f75-4af4-8337-a5bd28c26fb7	2026-08-31	Warnings	Exact identifier application number: M001
Kroger Extra Strength Assorted Fruit	CALCIUM CARBONATE	KROGER COMPANY	486d7a5f-cbc8-4f86-b12e-c5325bd8c62d	2026-08-31	Warnings	Exact identifier application number: M001
GERI-LANTA MAXIMUM STRENGTH	ALUMINUM HYDROXIDE, MAGNESIUM HYDROXIDE, DIMETHICONE	Preferred Pharmaceuticals Inc.	3b049027-30ac-4c78-a4f1-8191f7ed45bf	2026-08-27	Warnings	Exact identifier application number: M001
Extra Strength Gas Relief	SIMETHICONE	Shield Pharmaceuticals Corp	534144be-fcaf-400d-b772-595c62ae6ea6	2026-08-27	Warnings	Exact identifier application number: M001
Antacid	ALUMINUM HYDROXIDE, MAGNESIUM HYDROXIDE, SIMETHICONE	Guardian Drug Company	48ec50ab-f24b-367b-e063-6294a90ad736	2026-08-27	Warnings	Exact identifier application number: M001
REGULAR STRENGTH ANTACID	ALUMINUM HYDROXIDE, MAGNESIUM HYDROXIDE, DIMETHICONE	KROGER COMPANY	b9e61a03-e008-50ab-e053-2a95a90a3210	2026-08-26	Warnings	Exact identifier application number: M001
MAXIMUM STRENGTH ANTACID	ALUMINUM HYDROXIDE, MAGNESIUM HYDROXIDE, DIMETHICONE	CVS PHARMACY	af71e02d-e7c7-f925-e053-2995a90a0861	2026-08-26	Warnings	Exact identifier application number: M001
Tumeez Organic Apple	CALCIUM CARBONATE	BFY LLC	f561685a-5260-59c6-e053-2a95a90ae206	2026-08-25	Warnings	Exact identifier application number: M001
Dr. Sana Lemon Alivio Digestivo UPSET STOMACH	EFFERVESCENT ANTACID	EVI LABS	59cdf417-e5c0-6bb2-e063-6294a90a9c51	2026-08-24	Warnings	Exact identifier application number: M001
Dr Sana Alivio Digestivo Naranja UPSET STOMACH	EFFERVESCENT ANTACID	EVI LABS	59d07c2d-ef11-bd32-e063-6394a90af87d	2026-08-24	Warnings	Exact identifier application number: M001
Genexa Antacid Maximum Strength	CALCIUM CARBONATE	Genexa Inc.	3a39d91c-2dcd-71d6-e063-6394a90a5474	2026-08-22	Warnings	Exact identifier application number: M001
Mag-AL Plus	ALUMINUM HYDROXIDE, MAGNESIUM HYDROXIDE, AND SIMETHICONE	PAI Holdings, LLC dba PAI Pharma	896ab07a-1b40-43ab-8589-3be86b1c4198	2026-08-19	Warnings	Exact identifier application number: M001
CVS Health Extra Strength Antacid	ALUMINUM HYDROXIDE AND MAGNESIUM CARBONATE	CVS PHARMACY	8629529e-4363-4d37-9ae0-27193868df32	2026-08-19	Warnings	Exact identifier application number: M001
Mylanta Fall Harvest Collection Spiced Apple Cider	CALCIUM CARBONATE,MAGNESIUM HYDROXIDE AND SIMETHICONE	Infirst Healthcare Inc.	5a6040ff-1779-3215-e063-6294a90aaab1	2026-08-15	Warnings	Exact identifier application number: M001
Mylanta Fall Harvest Collection Pumpkin Spice	CALCIUM CARBONATE,MAGNESIUM HYDROXIDE AND SIMETHICONE	Infirst Healthcare Inc.	5a60a221-5b37-806e-e063-6394a90a5ccc	2026-08-15	Warnings	Exact identifier application number: M001
CVS Naturals	CALCIUM CARBONATE	CVS PHARMACY	899f057a-914d-49ca-a9fd-9fc48149782a	2026-08-14	Warnings	Exact identifier application number: M001

UNII, Preferred term, Registry number table
UNII	Preferred term	Registry number	Matched term
62TEY51RR1	BISMUTH SUBSALICYLATE	14882-18-9	BISMUTH SUBSALICYLATE

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	DailyMed	SPL version
308762	bismuth subsalicylate 525 MG in 30 mL Oral Suspension	PSN	05e14009-b35d-4711-b6f0-89b6d060b387	7
308762	bismuth subsalicylate 17.5 MG/ML Oral Suspension	SCD	05e14009-b35d-4711-b6f0-89b6d060b387	7
308762	bismuth subsalicylate 1.75 % Oral Suspension	SY	05e14009-b35d-4711-b6f0-89b6d060b387	7
308762	bismuth subsalicylate 262 MG per 15 ML Oral Suspension	SY	05e14009-b35d-4711-b6f0-89b6d060b387	7
308762	bismuth subsalicylate 524 MG per 30 ML Oral Suspension	SY	05e14009-b35d-4711-b6f0-89b6d060b387	7
308762	bismuth subsalicylate 525 MG per 30 ML Oral Suspension	SY	05e14009-b35d-4711-b6f0-89b6d060b387	7

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
66715-6855-4	66715685504	237 mL in 1 BOTTLE, PLASTIC (66715-6855-4)	237 ml	2020-06-01	0000-00-00	No	No	Current