Equaline tussin

Product NDC: 41163-359
11-digit product format: 411630359
Labeler code: 41163
Product ID: 41163-359_cbf1d837-f65d-4ed4-a9b7-41027b72120e
Type: HUMAN OTC DRUG
Nonproprietary name: Dextromethorphan HBr, Guaifenesin
Dosage form: SOLUTION
Route: ORAL
Labeler: Supervalu Inc
Application: part341
Marketing category: OTC MONOGRAPH FINAL
Marketing start: 2004-08-24
Marketing end: 0000-00-00
Substance: DEXTROMETHORPHAN HYDROBROMIDE; GUAIFENESIN
Active strength: 20 mg/10mL; mg/10mL
NDC exclude flag: No
Listing certified through: 2020-12-31
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 · 3 matching rows.

Dataset, Scope, Product NDC table
Dataset	Scope	Product NDC	Package NDC	Code	Status	Source date
excluded product	product	41163-359		D	Discontinued by firm	2026-10-16
excluded package	package	41163-359	41163-359-26	D	Discontinued by firm	2026-10-16
excluded package	package	41163-359	41163-359-34	D	Discontinued by firm	2026-10-16

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 · 32 matching rows.

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

Captured / source date, Dataset, Scope table
Captured / source date	Dataset	Scope	Package NDC	Snapshot	Source SHA-256
2025-12-14 17:58 UTC · source 2025-12-05	excluded product	product		`d630ba8d3edf…`	`732f749b63fb…`
2025-12-14 17:58 UTC · source 2025-12-05	excluded package	package	41163-359-26	`d630ba8d3edf…`	`732f749b63fb…`
2025-12-14 17:58 UTC · source 2025-12-05	excluded package	package	41163-359-34	`d630ba8d3edf…`	`732f749b63fb…`
2025-08-27 00:01 UTC · source 2025-08-26	excluded product	product		`f5e01cc5f278…`	`a2eaf40c39c3…`
2025-08-27 00:01 UTC · source 2025-08-26	excluded package	package	41163-359-26	`f5e01cc5f278…`	`a2eaf40c39c3…`
2025-08-27 00:01 UTC · source 2025-08-26	excluded package	package	41163-359-34	`f5e01cc5f278…`	`a2eaf40c39c3…`
2025-04-01 02:39 UTC · source 2025-03-31	excluded product	product		`2ef7874e63bc…`	`57b86245f4fa…`
2025-04-01 02:39 UTC · source 2025-03-31	excluded package	package	41163-359-26	`2ef7874e63bc…`	`57b86245f4fa…`
2025-04-01 02:39 UTC · source 2025-03-31	excluded package	package	41163-359-34	`2ef7874e63bc…`	`57b86245f4fa…`
2025-03-28 20:22 UTC · source 2025-03-28	excluded product	product		`a1b67e2a42f9…`	`c4cf2c586c0d…`
2025-03-28 20:22 UTC · source 2025-03-28	excluded package	package	41163-359-26	`a1b67e2a42f9…`	`c4cf2c586c0d…`
2025-03-28 20:22 UTC · source 2025-03-28	excluded package	package	41163-359-34	`a1b67e2a42f9…`	`c4cf2c586c0d…`
2025-03-22 03:12 UTC · source 2025-03-21	excluded product	product		`cfe11265f3b6…`	`090c488252e2…`
2025-03-22 03:12 UTC · source 2025-03-21	excluded package	package	41163-359-26	`cfe11265f3b6…`	`090c488252e2…`
2025-03-22 03:12 UTC · source 2025-03-21	excluded package	package	41163-359-34	`cfe11265f3b6…`	`090c488252e2…`
2025-03-10 12:48 UTC · source 2025-03-10	excluded product	product		`cdf11ea48f46…`	`ba0047e9e063…`
2025-03-10 12:48 UTC · source 2025-03-10	excluded package	package	41163-359-26	`cdf11ea48f46…`	`ba0047e9e063…`
2025-03-10 12:48 UTC · source 2025-03-10	excluded package	package	41163-359-34	`cdf11ea48f46…`	`ba0047e9e063…`
2025-02-02 03:52 UTC · source 2025-01-31	excluded product	product		`302b2466d912…`	`e7b80fea0513…`
2025-02-02 03:52 UTC · source 2025-01-31	excluded package	package	41163-359-26	`302b2466d912…`	`e7b80fea0513…`
2025-02-02 03:52 UTC · source 2025-01-31	excluded package	package	41163-359-34	`302b2466d912…`	`e7b80fea0513…`
2025-01-20 13:05 UTC · source 2025-01-20	excluded product	product		`ed331223b511…`	`672a5bd82f5f…`
2025-01-20 13:05 UTC · source 2025-01-20	excluded package	package	41163-359-26	`ed331223b511…`	`672a5bd82f5f…`
2025-01-20 13:05 UTC · source 2025-01-20	excluded package	package	41163-359-34	`ed331223b511…`	`672a5bd82f5f…`
2025-01-11 03:41 UTC · source 2025-01-10	excluded product	product		`0efc9e666f02…`	`f202fb6c5f17…`
2025-01-11 03:41 UTC · source 2025-01-10	excluded package	package	41163-359-26	`0efc9e666f02…`	`f202fb6c5f17…`
2025-01-11 03:41 UTC · source 2025-01-10	excluded package	package	41163-359-34	`0efc9e666f02…`	`f202fb6c5f17…`
2024-11-09 02:27 UTC · source 2024-11-08	excluded product	product		`ad56d346431e…`	`cc804d4bbf1e…`
2024-11-09 02:27 UTC · source 2024-11-08	excluded package	package	41163-359-26	`ad56d346431e…`	`cc804d4bbf1e…`
2024-11-09 02:27 UTC · source 2024-11-08	excluded package	package	41163-359-34	`ad56d346431e…`	`cc804d4bbf1e…`
2024-10-04 04:10 UTC · source 2024-10-03	excluded package	package	41163-359-34	`367a005e9d99…`	`383a685ebd0f…`
2024-07-10 04:00 UTC · source 2024-07-09	excluded package	package	41163-359-34	`557ba5c1ecfa…`	`9c80585c8c6e…`

Reported adverse events (FAERS/openFDA)#

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

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDC	Billing unit	Product NDC	DailyMed indexing SPL	SPL version	Effective
41163-359-26	ML - Milliliter	41163-359	0ea41c6c-90df-4a72-a1f4-94c59453538a	1	2016-07-19
41163-359-34	ML - Milliliter	41163-359	ad233ea3-0a14-4e00-bb0b-dac974a5e9ea	1	2013-02-13

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	DailyMed label	SPL version
DEXTROMETHORPHAN HYDROBROMIDE	ACTIVE INGREDIENT	9D2RTI9KYH	EQUALINE TUSSIN ADULT (DEXTROMETHORPHAN HBR, GUAIFENESIN) SOLUTION [SUPERVALU INC]	3
GUAIFENESIN	ACTIVE INGREDIENT	495W7451VQ	EQUALINE TUSSIN ADULT (DEXTROMETHORPHAN HBR, GUAIFENESIN) SOLUTION [SUPERVALU INC]	3
DEXTROMETHORPHAN	ACTIVE MOIETY	7355X3ROTS	EQUALINE TUSSIN ADULT (DEXTROMETHORPHAN HBR, GUAIFENESIN) SOLUTION [SUPERVALU INC]	3
GUAIFENESIN	ACTIVE MOIETY	495W7451VQ	EQUALINE TUSSIN ADULT (DEXTROMETHORPHAN HBR, GUAIFENESIN) SOLUTION [SUPERVALU INC]	3
ANHYDROUS CITRIC ACID	INACTIVE INGREDIENT	XF417D3PSL	EQUALINE TUSSIN ADULT (DEXTROMETHORPHAN HBR, GUAIFENESIN) SOLUTION [SUPERVALU INC]	3
FD&C RED NO. 40	INACTIVE INGREDIENT	WZB9127XOA	EQUALINE TUSSIN ADULT (DEXTROMETHORPHAN HBR, GUAIFENESIN) SOLUTION [SUPERVALU INC]	3
GLYCERIN	INACTIVE INGREDIENT	PDC6A3C0OX	EQUALINE TUSSIN ADULT (DEXTROMETHORPHAN HBR, GUAIFENESIN) SOLUTION [SUPERVALU INC]	3
HIGH FRUCTOSE CORN SYRUP	INACTIVE INGREDIENT	XY6UN3QB6S	EQUALINE TUSSIN ADULT (DEXTROMETHORPHAN HBR, GUAIFENESIN) SOLUTION [SUPERVALU INC]	3
MENTHOL	INACTIVE INGREDIENT	L7T10EIP3A	EQUALINE TUSSIN ADULT (DEXTROMETHORPHAN HBR, GUAIFENESIN) SOLUTION [SUPERVALU INC]	3
PROPYLENE GLYCOL	INACTIVE INGREDIENT	6DC9Q167V3	EQUALINE TUSSIN ADULT (DEXTROMETHORPHAN HBR, GUAIFENESIN) SOLUTION [SUPERVALU INC]	3
SODIUM BENZOATE	INACTIVE INGREDIENT	OJ245FE5EU	EQUALINE TUSSIN ADULT (DEXTROMETHORPHAN HBR, GUAIFENESIN) SOLUTION [SUPERVALU INC]	3
SODIUM CITRATE	INACTIVE INGREDIENT	1Q73Q2JULR	EQUALINE TUSSIN ADULT (DEXTROMETHORPHAN HBR, GUAIFENESIN) SOLUTION [SUPERVALU INC]	3
SUCRALOSE	INACTIVE INGREDIENT	96K6UQ3ZD4	EQUALINE TUSSIN ADULT (DEXTROMETHORPHAN HBR, GUAIFENESIN) SOLUTION [SUPERVALU INC]	3
WATER	INACTIVE INGREDIENT	059QF0KO0R	EQUALINE TUSSIN ADULT (DEXTROMETHORPHAN HBR, GUAIFENESIN) SOLUTION [SUPERVALU INC]	3

UNII, Preferred term, Registry number table
UNII	Preferred term	Registry number	Matched term
9D2RTI9KYH	DEXTROMETHORPHAN HYDROBROMIDE	6700-34-1	DEXTROMETHORPHAN HYDROBROMIDE
495W7451VQ	GUAIFENESIN	93-14-1	GUAIFENESIN

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
41163-359-26	41163035926	1 BOTTLE in 1 CARTON (41163-359-26) > 118 mL in 1 BOTTLE	1 bottle	2004-08-24	0000-00-00	No	No	Current
41163-359-34	41163035934	1 BOTTLE in 1 CARTON (41163-359-34) > 237 mL in 1 BOTTLE	1 bottle	2004-08-30	0000-00-00	No	No	Current

Title, Manufacturer, Effective date table
Title	Manufacturer	Effective date	Type	Version
SuperValu Inc. Adult Tussin Drug Facts	United Natural Foods, Inc. dba UNFI	2023-07-20	HUMAN OTC DRUG LABEL	5