Cough Relief

Product NDC: 15127-309
11-digit product format: 151270309
Labeler code: 15127
Product ID: 15127-309_ac6b288b-45f0-4fd3-a692-af2e1f1d4435
Type: HUMAN OTC DRUG
Nonproprietary name: Dextromethorphan HBr
Dosage form: LIQUID
Route: ORAL
Labeler: Select Brand Dist.
Application: part341
Marketing category: OTC MONOGRAPH FINAL
Marketing start: 2015-06-30
Marketing end: 2020-12-31
Substance: DEXTROMETHORPHAN HYDROBROMIDE
Active strength: 15 mg/5mL
NDC exclude flag: No
Listing certified through: 0000-00-00
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 · 2 matching rows.

Dataset, Scope, Product NDC table
Dataset	Scope	Product NDC	Package NDC	Code	Status	Reporting period	Source date
excluded product	product	15127-309		D	Discontinued by firm		2026-10-15
excluded package	package	15127-309	15127-309-04	D	Discontinued by firm		2026-10-15

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 · 24 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	15127-309-04	`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	15127-309-04	`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	15127-309-04	`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	15127-309-04	`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	15127-309-04	`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	15127-309-04	`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	15127-309-04	`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	15127-309-04	`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	15127-309-04	`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	15127-309-04	`ad56d346431e…`	`cc804d4bbf1e…`
2024-10-04 04:10 UTC · source 2024-10-03	excluded product	product		`367a005e9d99…`	`383a685ebd0f…`
2024-10-04 04:10 UTC · source 2024-10-03	excluded package	package	15127-309-04	`367a005e9d99…`	`383a685ebd0f…`
2024-07-10 04:00 UTC · source 2024-07-09	excluded product	product		`557ba5c1ecfa…`	`9c80585c8c6e…`
2024-07-10 04:00 UTC · source 2024-07-09	excluded package	package	15127-309-04	`557ba5c1ecfa…`	`9c80585c8c6e…`

Reported adverse events (FAERS/openFDA)#

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

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	DailyMed label	SPL version
DEXTROMETHORPHAN HYDROBROMIDE	ACTIVE INGREDIENT	9D2RTI9KYH	COUGH RELIEF ADULT (DEXTROMETHORPHAN HBR) LIQUID [SELECT BRAND DIST.]	1
DEXTROMETHORPHAN	ACTIVE MOIETY	7355X3ROTS	COUGH RELIEF ADULT (DEXTROMETHORPHAN HBR) LIQUID [SELECT BRAND DIST.]	1
ANHYDROUS CITRIC ACID	INACTIVE INGREDIENT	XF417D3PSL	COUGH RELIEF ADULT (DEXTROMETHORPHAN HBR) LIQUID [SELECT BRAND DIST.]	1
EDETATE DISODIUM	INACTIVE INGREDIENT	7FLD91C86K	COUGH RELIEF ADULT (DEXTROMETHORPHAN HBR) LIQUID [SELECT BRAND DIST.]	1
FD&C YELLOW NO. 6	INACTIVE INGREDIENT	H77VEI93A8	COUGH RELIEF ADULT (DEXTROMETHORPHAN HBR) LIQUID [SELECT BRAND DIST.]	1
GLYCERIN	INACTIVE INGREDIENT	PDC6A3C0OX	COUGH RELIEF ADULT (DEXTROMETHORPHAN HBR) LIQUID [SELECT BRAND DIST.]	1
HIGH FRUCTOSE CORN SYRUP	INACTIVE INGREDIENT	XY6UN3QB6S	COUGH RELIEF ADULT (DEXTROMETHORPHAN HBR) LIQUID [SELECT BRAND DIST.]	1
HYDROXYETHYL CELLULOSE (1500 MPA.S AT 1%)	INACTIVE INGREDIENT	L605B5892V	COUGH RELIEF ADULT (DEXTROMETHORPHAN HBR) LIQUID [SELECT BRAND DIST.]	1
POLYETHYLENE GLYCOLS	INACTIVE INGREDIENT	3WJQ0SDW1A	COUGH RELIEF ADULT (DEXTROMETHORPHAN HBR) LIQUID [SELECT BRAND DIST.]	1
PROPYLENE GLYCOL	INACTIVE INGREDIENT	6DC9Q167V3	COUGH RELIEF ADULT (DEXTROMETHORPHAN HBR) LIQUID [SELECT BRAND DIST.]	1
SODIUM BENZOATE	INACTIVE INGREDIENT	OJ245FE5EU	COUGH RELIEF ADULT (DEXTROMETHORPHAN HBR) LIQUID [SELECT BRAND DIST.]	1
SUCRALOSE	INACTIVE INGREDIENT	96K6UQ3ZD4	COUGH RELIEF ADULT (DEXTROMETHORPHAN HBR) LIQUID [SELECT BRAND DIST.]	1
SUCROSE	INACTIVE INGREDIENT	C151H8M554	COUGH RELIEF ADULT (DEXTROMETHORPHAN HBR) LIQUID [SELECT BRAND DIST.]	1
WATER	INACTIVE INGREDIENT	059QF0KO0R	COUGH RELIEF ADULT (DEXTROMETHORPHAN HBR) LIQUID [SELECT BRAND DIST.]	1
XANTHAN GUM	INACTIVE INGREDIENT	TTV12P4NEE	COUGH RELIEF ADULT (DEXTROMETHORPHAN HBR) LIQUID [SELECT BRAND DIST.]	1

Cough Relief

NDC auxiliary status#

Observed NDC auxiliary status history#

Reported adverse events (FAERS/openFDA)#

DailyMed Socrata Ingredients#

Related Records#

Related UNII Ingredients#

Related DailyMed Labels#