Quality Choice Mucus Relief

Product NDC: 63868-998
11-digit product format: 638680998
Labeler code: 63868
Product ID: 63868-998_e8f6721f-0337-445c-84b2-592329d0ba32
Type: HUMAN OTC DRUG
Nonproprietary name: Guaifenesin
Dosage form: TABLET
Route: ORAL
Labeler: Chain Drug Marketing Association
Application: M012
Marketing category: OTC MONOGRAPH DRUG
Marketing start: 2012-08-01
Substance: GUAIFENESIN
Active strength: 400 mg/1
Pharmacologic classes: Decreased Respiratory Secretion Viscosity [PE], Expectorant [EPC], Increased Respiratory Secretions [PE]
NDC exclude flag: No
Listing certified through: 2026-12-31
Current FDA listing: Yes

Additional Listing Data#

Ingredient, Strength table
Ingredient	Strength
GUAIFENESIN	400 mg/1

Field, Values table
Field	Values
Unii	495W7451VQ
Rxcui	359601

Product concept, Relation, Version table
Product concept	Relation	Version	Effective
4fe95224-f543-4dbb-9445-8cca122b48c8	Product name	1	20150609
e8718272-64cb-4436-969b-176c3067c8f4	Product name	1	20150609
106ff02a-57e1-4c4c-a307-fd582ff4e311	Product name	1	20150212

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
63868-998-50	2021-05-05	C162847	48780-1	9d75b9d0-a86a-f424-e053-dadaa90a57ce	Drug Facts
63868-998-50	2020-01-31	C162847	48780-1	9d75b9d0-a86a-f424-e053-dadaa90a57ce	Drug Facts

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
63868-998-50	Quality Choice Mucus Relief	1 in 1 CARTON	TABLET	1		4
63868-998-50	Quality Choice Mucus Relief	50 in 1 BOTTLE	TABLET	50		4

Package NDC, Billing unit, Product NDC table
Package NDC	Billing unit	Product NDC	DailyMed indexing SPL	SPL version	Effective
63868-998-50	EA - Each	63868-998	5e5affd7-ff26-4bb8-8085-d626098c89e3	1	2017-04-05

Ingredient, Type, UNII table
Ingredient	Type	UNII	DailyMed label	SPL version
Guaifenesin	ACTIVE INGREDIENT	495W7451VQ	QUALITY CHOICE MUCUS RELIEF (GUAIFENESIN) TABLET [CHAIN DRUG MARKETING ASSOCIATION]	1
Guaifenesin	ACTIVE MOIETY	495W7451VQ	QUALITY CHOICE MUCUS RELIEF (GUAIFENESIN) TABLET [CHAIN DRUG MARKETING ASSOCIATION]	1
COPOVIDONE	INACTIVE INGREDIENT	D9C330MD8B	QUALITY CHOICE MUCUS RELIEF (GUAIFENESIN) TABLET [CHAIN DRUG MARKETING ASSOCIATION]	1
MAGNESIUM STEARATE	INACTIVE INGREDIENT	70097M6I30	QUALITY CHOICE MUCUS RELIEF (GUAIFENESIN) TABLET [CHAIN DRUG MARKETING ASSOCIATION]	1
MALTODEXTRIN	INACTIVE INGREDIENT	7CVR7L4A2D	QUALITY CHOICE MUCUS RELIEF (GUAIFENESIN) TABLET [CHAIN DRUG MARKETING ASSOCIATION]	1
SILICON DIOXIDE	INACTIVE INGREDIENT	ETJ7Z6XBU4	QUALITY CHOICE MUCUS RELIEF (GUAIFENESIN) TABLET [CHAIN DRUG MARKETING ASSOCIATION]	1
STEARIC ACID	INACTIVE INGREDIENT	4ELV7Z65AP	QUALITY CHOICE MUCUS RELIEF (GUAIFENESIN) TABLET [CHAIN DRUG MARKETING ASSOCIATION]	1

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
63868-998	QUALITY CHOICE MUCUS RELIEF (GUAIFENESIN) TABLET [CHAIN DRUG MARKETING ASSOCIATION]	4	Current NDC, Legacy NDC, 2 package rows	20241220_41f88b43-3e0a-4650-b167-a72afe6177e8.zip

UNII, Preferred term, Registry number table
UNII	Preferred term	Registry number	Matched term
495W7451VQ	GUAIFENESIN	93-14-1	GUAIFENESIN

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	DailyMed	SPL version
359601	guaiFENesin 400 MG Oral Tablet	PSN	41f88b43-3e0a-4650-b167-a72afe6177e8	4
359601	guaifenesin 400 MG Oral Tablet	SCD	41f88b43-3e0a-4650-b167-a72afe6177e8	4

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
63868-998-50	63868099850	1 BOTTLE in 1 CARTON (63868-998-50) / 50 TABLET in 1 BOTTLE	1 bottle	2012-08-01	0000-00-00	No	No	Current

Title, Manufacturer, Effective date table
Title	Manufacturer	Effective date	Type	Version
Drug Facts	Chain Drug Marketing Association \| Reese Pharmaceutical Co \| Pharbest	2024-12-18	HUMAN OTC DRUG LABEL	4