NDC 11673-704 - Multi Symptom Cold and Multi Symptom Nighttime Cold Childrens

This NDC is not currently matched to an FDA NDC product listing in FDA.report, but it is a valid NDC-form code. FDA.report is showing the available DailyMed label context for the product root.

Product NDC: 11673-704
Package NDCs from labels: 11673-704-04
Manufacturer: TARGET Corporation
Effective date: 2024-06-04
Current FDA listing: Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
Label	Manufacturer	Effective date	Type
Multi Symptom Cold Daytime Childrens - TARGET Corporation	TARGET Corporation	2024-06-04	HUMAN OTC DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
11673-704-04	Multi Symptom Cold and Multi Symptom Nighttime ColdChildrens	118 mL in 1 BOTTLE, PLASTIC	LIQUID	118 mL	5 mg in 5mL	5

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
11673-704	MULTI SYMPTOM COLD AND MULTI SYMPTOM NIGHTTIME COLD CHILDRENS (DEXTROMETHORPHAN HBR, GUAIFENESIN, PHENYLEPHRINE HCI, ACETAMINOPHEN, DIPHENHYDRAMINE HCI, PHENYLEPHRINE HCI) KIT [TARGET CORPORATION]	5	Unmatched	20240606_e3da3003-88e3-4431-8b65-e61e17728901.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 338 of 351 · 7,003 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Diphenhydramine HCl and Ibuprofen	DIPHENHYDRAMINE HCL AND IBUPROFEN	Aurohealth LLC	39af6dfa-e822-43a5-bd1a-338cf5da89ce	2022-12-09	Warnings	Exact identifier unii: TC2D6JAD40
Mucus Relief Extended Release Maximum Strength	GUAIFENESIN	H E B	6f075c29-8256-4cac-96c4-a772a53ad21d	2022-12-09	Warnings	Exact identifier unii: 495W7451VQ
Guaifenesin and Dextromethorphan HBr	GUAIFENESIN AND DEXTROMETHORPHAN HBR	PUBLIX SUPER MARKETS, INC	9870b7ee-2bfb-42f5-9762-77d2dd13434a	2022-12-06	Warnings	Exact identifier unii: 9D2RTI9KYH unii: 495W7451VQ
Guaifenesin and Dextromethorphan Hydrobromide HBR	GUAIFENESIN AND DEXTROMETHORPHAN HYDROBROMIDE	RITE-AID	2343f031-d658-498a-b5d1-6dcdb26b3cf0	2022-12-06	Warnings	Exact identifier unii: 9D2RTI9KYH unii: 495W7451VQ
Guaifenesin and Dextromethorphan HBr	GUAIFENESIN AND DEXTROMETHORPHAN HBR	SUN PHARMACEUTICAL INDUSTRIES, INC.	06328741-03e3-49cf-ae44-d4c2116e38a3	2022-12-06	Warnings	Exact identifier unii: 9D2RTI9KYH unii: 495W7451VQ
MAXIMUM STRENGTH Mucus D	GUAIFENESIN AND PSEUDOEPHEDRINE HYDROCHLORIDE	CVS Pharmacy	9a560b80-972c-4af5-8fe8-eaef0b0d83b3	2022-12-01	Warnings	Exact identifier unii: 495W7451VQ
Refresh Digital PF	CARBOXYMETHYLCELLULOSE SODIUM, GLYCERIN AND POLYSORBATE 80	Allergan, Inc.	97e83e68-6374-4df4-93f6-d707fc32748d	2022-11-28	Warnings	Exact identifier unii: PDC6A3C0OX
Refresh Digital	CARBOXYMETHYLCELLULOSE SODIUM, GLYCERIN, POLYSORBATE 80	Allergan, Inc.	b2bd34d4-fab9-4f4b-9be2-5d30b55f5b81	2022-11-28	Warnings	Exact identifier unii: PDC6A3C0OX
GUAIFENESIN	GUAIFENESIN	CVS	4efa8bf9-3394-47b4-b630-9476b15d2dfc	2022-11-23	Warnings	Exact identifier unii: 495W7451VQ
Mucus Relief Extended Release	GUAIFENESIN	Care One (American Sales Company)	96569c70-0936-4041-ab32-2b2262402f34	2022-11-21	Warnings	Exact identifier unii: 495W7451VQ
Mucus Relief Maximum Strength	GUAIFENESIN	Care One (American Sales Company)	c94e3943-20da-4bd4-b0ff-6aa60b03a1bf	2022-11-21	Warnings	Exact identifier unii: 495W7451VQ
Mucus Relief	GUAIFENESIN	McKesson Corporation dba SKY Packaging	69b61f05-8f0b-420f-b4ef-df933b70eebc	2022-11-21	Warnings	Exact identifier unii: 495W7451VQ
DG health mucus dm	DEXTROMETHORPHAN HBR, GUAIFENESIN	Dolgencorp, LLC	add72ca5-94cd-437f-b30f-6149c08b5f21	2022-11-14	Warnings	Exact identifier unii: 9D2RTI9KYH unii: 495W7451VQ
Mucus Relief	GUAIFENESIN	H E B	562b6ab6-4795-4909-8008-e919173844c9	2022-11-07	Warnings	Exact identifier unii: 495W7451VQ
DAYTIME-NIGHTTIME SEVERE COLD AND FLU	ACETAMINOPHEN, DEXTROMETHORPHAN HBR, DOXYLAMINE SUCCINATE, PHENYLEPHRINE HCL	KROGER	a2508699-08c0-4a22-e053-2a95a90a8a6d	2022-11-02	Warnings	Exact identifier application number: M012
Anticoagulant Citrate Phosphate Dextrose (CPD) Blood-Pack Units in PL 146 Plastic	ANTICOAGULANT CITRATE PHOSPHATE DEXTROSE (CPD) SOLUTION	Fenwal, Inc.	d55cb701-9664-4931-8754-1a8cae68da06	2022-11-01		Exact identifier unii: XF417D3PSL
Oxycodone and Acetaminophen	OXYCODONE AND ACETAMINOPHEN	Proficient Rx LP	78933d4a-d78a-43bc-9052-a032901ee050	2022-11-01	Boxed warning, Warnings, Adverse reactions	Exact identifier unii: 362O9ITL9D
CPDA-1	ANTICOAGULANT CITRATE PHOSPHATE DEXTROSE ADENINE (CPDA-1) SOLUTION	Fenwal, Inc.	f9d7f1b4-7a77-44f9-8924-10b16008b49d	2022-11-01		Exact identifier unii: XF417D3PSL
Oxycodone and Acetaminophen	OXYCODONE AND ACETAMINOPHEN	Proficient Rx LP	5df7c033-0f31-45bc-8c34-3da45635e66d	2022-11-01	Boxed warning, Warnings, Adverse reactions	Exact identifier unii: 362O9ITL9D
Anticoagulant Citrate Phosphate Dextrose (CPD) Blood-Pack Units in PL 146 Plastic	ANTICOAGULANT CITRATE PHOSPHATE DEXTROSE (CPD)	Fenwal, Inc.	4a08a9ec-46a5-4fcf-80ee-5c33f1a8b746	2022-11-01		Exact identifier unii: XF417D3PSL

Reported adverse events (FAERS/openFDA)#

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