Vicks DayQuil

Product NDC: 37000-565
Requested package NDC: 37000-565-12
11-digit product format: 370000565
Labeler code: 37000
Product ID: 37000-565_bb165180-2e86-d169-e053-2a95a90ac600
Type: HUMAN OTC DRUG
Nonproprietary name: Dextromethorphan Hydrobromide
Dosage form: LIQUID
Route: ORAL
Labeler: The Procter & Gamble Manufacturing Company
Application: part341
Marketing category: OTC MONOGRAPH FINAL
Marketing start: 2011-06-22
Marketing end: 0000-00-00
Substance: DEXTROMETHORPHAN HYDROBROMIDE
Active strength: 15 mg/15mL
NDC exclude flag: No
Listing certified through: 2022-12-31
Current FDA listing: Historical FDA.report record

NDC auxiliary status#

These records are reproduced from FDA’s unfinished, excluded, and compounder listings. They describe what appeared in the source files; a missing record does not establish a regulatory status. View all current auxiliary records, including entries without an NDC. · View the auxiliary file history.

Current NDC status page 1 of 1 · 1 matching rows.

Dataset, Scope, Product NDC table
Dataset	Scope	Product NDC	Package NDC	Code	Status	Reporting period	Source date
excluded package	package	37000-565	37000-565-12	D	Discontinued by firm		2026-10-05

Observed NDC auxiliary status history#

This history shows the information present in each captured FDA auxiliary file. It is not a continuous regulatory timeline, and a missing record does not establish a status.

Historic NDC status page 1 of 1 · 12 matching rows.

View current auxiliary records. · View the auxiliary file history.

Captured / source date, Snapshot, Source SHA-256 table
Captured / source date	Snapshot	Source SHA-256
2025-12-14 17:58 UTC · source 2025-12-05	`d630ba8d3edf…`	`732f749b63fb…`
2025-08-27 00:01 UTC · source 2025-08-26	`f5e01cc5f278…`	`a2eaf40c39c3…`
2025-04-01 02:39 UTC · source 2025-03-31	`2ef7874e63bc…`	`57b86245f4fa…`
2025-03-28 20:22 UTC · source 2025-03-28	`a1b67e2a42f9…`	`c4cf2c586c0d…`
2025-03-22 03:12 UTC · source 2025-03-21	`cfe11265f3b6…`	`090c488252e2…`
2025-03-10 12:48 UTC · source 2025-03-10	`cdf11ea48f46…`	`ba0047e9e063…`
2025-02-02 03:52 UTC · source 2025-01-31	`302b2466d912…`	`e7b80fea0513…`
2025-01-20 13:05 UTC · source 2025-01-20	`ed331223b511…`	`672a5bd82f5f…`
2025-01-11 03:41 UTC · source 2025-01-10	`0efc9e666f02…`	`f202fb6c5f17…`
2024-11-09 02:27 UTC · source 2024-11-08	`ad56d346431e…`	`cc804d4bbf1e…`
2024-10-04 04:10 UTC · source 2024-10-03	`367a005e9d99…`	`383a685ebd0f…`
2024-07-10 04:00 UTC · source 2024-07-09	`557ba5c1ecfa…`	`9c80585c8c6e…`

Reported adverse events (FAERS/openFDA)#

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

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Related label table
NDC	Effective	Related label
37000-565-08	2021-02-11	VICKS ® DayQuil ® COUGH
37000-565-12	2021-02-11	VICKS ® DayQuil ® COUGH
37000-565-08	2021-01-29	VICKS ® DayQuil ® COUGH
37000-565-12	2021-01-29	VICKS ® DayQuil ® COUGH

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDC	Billing unit	Product NDC	DailyMed indexing SPL	SPL version	Effective
37000-565-12	ML - Milliliter	37000-565	8aba0440-9411-4c00-bb01-b1e5ae1a8785	1	2013-07-02

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	DailyMed label	SPL version
Dextromethorphan Hydrobromide	ACTIVE INGREDIENT	9D2RTI9KYH	VICKS DAYQUIL COUGH (DEXTROMETHORPHAN HYDROBROMIDE) LIQUID [THE PROCTER & GAMBLE MANUFACTURING COMPANY]	3
Dextromethorphan	ACTIVE MOIETY	7355X3ROTS	VICKS DAYQUIL COUGH (DEXTROMETHORPHAN HYDROBROMIDE) LIQUID [THE PROCTER & GAMBLE MANUFACTURING COMPANY]	3
citric acid monohydrate	INACTIVE INGREDIENT	2968PHW8QP	VICKS DAYQUIL COUGH (DEXTROMETHORPHAN HYDROBROMIDE) LIQUID [THE PROCTER & GAMBLE MANUFACTURING COMPANY]	3
D&C Yellow No. 10	INACTIVE INGREDIENT	35SW5USQ3G	VICKS DAYQUIL COUGH (DEXTROMETHORPHAN HYDROBROMIDE) LIQUID [THE PROCTER & GAMBLE MANUFACTURING COMPANY]	3
FD&C Yellow No. 6	INACTIVE INGREDIENT	H77VEI93A8	VICKS DAYQUIL COUGH (DEXTROMETHORPHAN HYDROBROMIDE) LIQUID [THE PROCTER & GAMBLE MANUFACTURING COMPANY]	3
high fructose corn syrup	INACTIVE INGREDIENT	XY6UN3QB6S	VICKS DAYQUIL COUGH (DEXTROMETHORPHAN HYDROBROMIDE) LIQUID [THE PROCTER & GAMBLE MANUFACTURING COMPANY]	3
polyethylene glycols	INACTIVE INGREDIENT	3WJQ0SDW1A	VICKS DAYQUIL COUGH (DEXTROMETHORPHAN HYDROBROMIDE) LIQUID [THE PROCTER & GAMBLE MANUFACTURING COMPANY]	3
propylene glycol	INACTIVE INGREDIENT	6DC9Q167V3	VICKS DAYQUIL COUGH (DEXTROMETHORPHAN HYDROBROMIDE) LIQUID [THE PROCTER & GAMBLE MANUFACTURING COMPANY]	3
saccharin sodium	INACTIVE INGREDIENT	SB8ZUX40TY	VICKS DAYQUIL COUGH (DEXTROMETHORPHAN HYDROBROMIDE) LIQUID [THE PROCTER & GAMBLE MANUFACTURING COMPANY]	3
sodium citrate	INACTIVE INGREDIENT	1Q73Q2JULR	VICKS DAYQUIL COUGH (DEXTROMETHORPHAN HYDROBROMIDE) LIQUID [THE PROCTER & GAMBLE MANUFACTURING COMPANY]	3
water	INACTIVE INGREDIENT	059QF0KO0R	VICKS DAYQUIL COUGH (DEXTROMETHORPHAN HYDROBROMIDE) LIQUID [THE PROCTER & GAMBLE MANUFACTURING COMPANY]	3

UNII, Preferred term, Registry number table
UNII	Preferred term	Registry number	Matched term
9D2RTI9KYH	DEXTROMETHORPHAN HYDROBROMIDE	6700-34-1	DEXTROMETHORPHAN HYDROBROMIDE

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
37000-565-12	37000056512	354 mL in 1 BOTTLE, PLASTIC (37000-565-12)	354 ml	2011-06-22	0000-00-00	No	No	Current

Title, Manufacturer, Effective date table
Title	Manufacturer	Effective date	Type	Version
Vicks ® DayQuil ® Tropical and Vicks ® NyQuil ® Cherry Cough	The Procter & Gamble Manufacturing Company	2021-02-12	HUMAN OTC DRUG LABEL	3
VICKS ® DayQuil ® COUGH	The Procter & Gamble Manufacturing Company	2021-02-11	HUMAN OTC DRUG LABEL	6