NDC 61715-014-50 - Preferred Plus Chest Congestion Relief PE

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: 61715-014
Requested NDC: 61715-014-50
Package NDCs from labels: 61715-014-50, 61715-014-01
Manufacturer: Kinray | Reese Pharmaceutical Co
Effective date: 2013-01-15
Current FDA listing: Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
Label	Manufacturer	Effective date	Type
Preferred Plus Chest Congestion Relief PE - Kinray \| Reese Pharmaceutical Co	Kinray \| Reese Pharmaceutical Co	2013-01-15	HUMAN OTC DRUG LABEL

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
61715-014-01	2020-02-19	C162847	48780-1	9d75b9cf-d865-f424-e053-dadaa90a57ce	DRUG FACTS
61715-014-01	2020-01-31	C162847	48780-1	9d75b9cf-d865-f424-e053-dadaa90a57ce	DRUG FACTS

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	DailyMed label	SPL version
Guaifenesin	ACTIVE INGREDIENT	495W7451VQ	PREFERRED PLUS CHEST CONGESTION RELIEF PE (GUAIFENESIN/PHENYLEPHRINE) TABLET [KINRAY]	1
PHENYLEPHRINE HYDROCHLORIDE	ACTIVE INGREDIENT	04JA59TNSJ	PREFERRED PLUS CHEST CONGESTION RELIEF PE (GUAIFENESIN/PHENYLEPHRINE) TABLET [KINRAY]	1
Guaifenesin	ACTIVE MOIETY	495W7451VQ	PREFERRED PLUS CHEST CONGESTION RELIEF PE (GUAIFENESIN/PHENYLEPHRINE) TABLET [KINRAY]	1
PHENYLEPHRINE	ACTIVE MOIETY	1WS297W6MV	PREFERRED PLUS CHEST CONGESTION RELIEF PE (GUAIFENESIN/PHENYLEPHRINE) TABLET [KINRAY]	1
CELLULOSE, MICROCRYSTALLINE	INACTIVE INGREDIENT	OP1R32D61U	PREFERRED PLUS CHEST CONGESTION RELIEF PE (GUAIFENESIN/PHENYLEPHRINE) TABLET [KINRAY]	1
CROSCARMELLOSE SODIUM	INACTIVE INGREDIENT	M28OL1HH48	PREFERRED PLUS CHEST CONGESTION RELIEF PE (GUAIFENESIN/PHENYLEPHRINE) TABLET [KINRAY]	1
LACTOSE	INACTIVE INGREDIENT	J2B2A4N98G	PREFERRED PLUS CHEST CONGESTION RELIEF PE (GUAIFENESIN/PHENYLEPHRINE) TABLET [KINRAY]	1
MAGNESIUM SILICATE	INACTIVE INGREDIENT	9B9691B2N9	PREFERRED PLUS CHEST CONGESTION RELIEF PE (GUAIFENESIN/PHENYLEPHRINE) TABLET [KINRAY]	1
MAGNESIUM STEARATE	INACTIVE INGREDIENT	70097M6I30	PREFERRED PLUS CHEST CONGESTION RELIEF PE (GUAIFENESIN/PHENYLEPHRINE) TABLET [KINRAY]	1
MALTODEXTRIN	INACTIVE INGREDIENT	7CVR7L4A2D	PREFERRED PLUS CHEST CONGESTION RELIEF PE (GUAIFENESIN/PHENYLEPHRINE) TABLET [KINRAY]	1
MINERAL OIL	INACTIVE INGREDIENT	T5L8T28FGP	PREFERRED PLUS CHEST CONGESTION RELIEF PE (GUAIFENESIN/PHENYLEPHRINE) TABLET [KINRAY]	1
POVIDONE	INACTIVE INGREDIENT	FZ989GH94E	PREFERRED PLUS CHEST CONGESTION RELIEF PE (GUAIFENESIN/PHENYLEPHRINE) TABLET [KINRAY]	1

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 8 of 114 · 2,279 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Stonarhini	CHLORPHENIRAMINE MALEATE, PHENYLEPHRINE	Sato Pharmaceutical Co., Ltd.	cc353280-0b4c-418c-93fe-850125955009	2026-07-31	Warnings	Exact identifier unii: 04JA59TNSJ
Vedlube	MINERAL OIL AND WHITE PETROLATUM LUBRICANT EYE OINTMENT	VEDCO INC	55d126fa-7489-4307-824e-b6957e57d4e9	2026-07-31	Warnings	Exact identifier unii: T5L8T28FGP
Rugby Mucus Relief DM ER	DEXTROMETHORPHAN HYDROBROMIDE, GUAIFENESIN	Rugby Laboratories	f2629794-4845-4ca6-8668-a21a56f182cb	2026-07-30	Warnings	Exact identifier unii: 495W7451VQ
Phenylephrine Hydrochloride	PHENYLEPHRINE HYDROCHLORIDE	Lifestar Pharma LLC	1767c4b7-36a0-4e64-9091-2af22161402f	2026-07-30	Warnings, Adverse reactions	Exact identifier unii: 04JA59TNSJ
Severe Congestion and Pain	ACETAMINOPHEN, GUAIFENESIN, PHENYLEPHRINE HCL	Family Dollar Services Inc	ce590997-3cae-4f22-ac39-2b14d39494bc	2026-07-30	Warnings	Exact identifier unii: 04JA59TNSJ unii: 495W7451VQ
up and up mucus relief dm	DEXTROMETHORPHAN HYDROBROMIDE, GUAIFENESIN	Target Corporation	9cb3719b-44bc-4ad1-a9c5-e6cc047f4d0e	2026-07-30	Warnings	Exact identifier unii: 495W7451VQ
Phenylephrine Hydrochloride	PHENYLEPHRINE HYDROCHLORIDE	Lifestar Pharma LLC	f43e4abd-0083-4fe5-9c27-0ba9245e5138	2026-07-30	Warnings, Adverse reactions	Exact identifier unii: 04JA59TNSJ
up and up	PHENYLEPHRINE HYDROCHLORIDE	Target Corporation	b42775ae-44fe-487e-b9ca-21d9687020a9	2026-07-29	Warnings	Exact identifier unii: 04JA59TNSJ
RUGBY MUCUS RELIEF DM ER	DEXTROMETHORPHAN HYDROBROMIDE, GUAIFENESIN	Rugby Laboratories	8090d561-0478-435d-ad6f-2334e1823bc3	2026-07-28	Warnings	Exact identifier unii: 495W7451VQ
Exchange Select Mucus DM	DEXTROMETHORPHAN HBR, GUAIFENESIN	Army & Air Force Exchange Service	99a11bea-8cf5-4c5d-95b1-eaedccaf9e7d	2026-07-28	Warnings	Exact identifier unii: 495W7451VQ
NIGHTTIME SEVERE COLD AND FLU	ACETAMINOPHEN, DEXTROMETHORPHAN HBR, DOXYLAMINE SUCCINATE, PHENYLEPHRINE HCL	CVS WOONSOCKET PRESCRIPTION CENTER, INCORPORATED	d1115a55-35cd-4f20-8872-f42983a5ebcd	2026-07-28	Warnings	Exact identifier unii: 04JA59TNSJ
TUSSIN	DEXTROMETHORPHAN HYDROBROMIDE, GUAIFENESIN	Safeway	a5e2bda4-2da6-4c20-855d-2888dadf0c3a	2026-07-28	Warnings	Exact identifier unii: 495W7451VQ
DM Maximum	DEXTROMETHORPHAN HBR, GUAIFENESIN	CVS WOONSOCKET PRESCRIPTION CENTER, INCORPORATED	f6029b04-e681-40fc-be4f-14091b76dd4e	2026-07-27	Warnings	Exact identifier unii: 495W7451VQ
Cold and Flu Severe	ACETAMINOPHEN, DEXTROMETHORPHAN HBR, PHENYLEPHRINE HCL, TRIPROLIDINE HCL	Walgreen Company	0a48f650-ad2a-4105-9ff4-2bc4d94b46d3	2026-07-27	Warnings	Exact identifier unii: 04JA59TNSJ
Cold and Flu	ACETAMINOPHEN, DEXTROMETHORPHAN HBR, GUAIFENESIN, PHENYLEPHRINE HCL	Walgreen Company	84202ebe-97b6-4be2-bb09-7f2729303f96	2026-07-27	Warnings	Exact identifier unii: 04JA59TNSJ unii: 495W7451VQ
Daytime Severe Cold and Flu Relief	ACETAMINOPHEN, DEXTROMETHORPHAN HBR, GUAIFENESIN, PHENYLEPHRINE HCL	Rite Aid Corporation	8d41defe-8120-4cbb-b42e-c805cc5a794b	2026-07-24	Warnings	Exact identifier unii: 04JA59TNSJ unii: 495W7451VQ
Acetaminophen, Dextromethorphan Hydrobromide and Phenylephrine Hydrochloride	ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE AND PHENYLEPHRINE HYDROCHLORIDE	Prodose, Inc.	3afc88c7-388a-dbd9-e063-6294a90a4faf	2026-07-24	Warnings	Exact identifier unii: 04JA59TNSJ
SERYNTH HEMORRHOID	LIDOCAINE 4% PHENYLEPHRINE HCL 0.25% HEMORRHOID	Jiangxi Yudexi Pharmaceutical Co., LTD	4c667f3d-1238-2f02-e063-6394a90ab742	2026-07-24	Warnings	Exact identifier unii: 04JA59TNSJ
DERMFREE HEMORRHOID	LIDOCAINE 4% PHENYLEPHRINE HCL 0.25% HEMORRHOID	Jiangxi Yudexi Pharmaceutical Co., LTD	4a5d0e79-d620-0147-e063-6294a90a3103	2026-07-23	Warnings	Exact identifier unii: 04JA59TNSJ
Giltuss Allergy Plus	CHLOPHEDIANOL HCL, CHLORPHENIRAMINE MALEATE, PHENYLEPHRINE HCL	Gil Pharmaceutical Corp	85a0dc7f-ffb5-7d52-e053-2991aa0a602a	2026-07-23	Warnings	Exact identifier unii: 04JA59TNSJ

Reported adverse events (FAERS/openFDA)#

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