COUGH MEDICINE

Product NDC: 76206-002
11-digit product format: 762060002
Labeler code: 76206
Product ID: 76206-002_a6d057b3-f01b-c377-e053-2995a90a41b0
Type: HUMAN OTC DRUG
Nonproprietary name: Dextromethorphan
Dosage form: LIQUID
Route: ORAL
Labeler: RFX Pharmaceutical Co., Ltd.
Application: part341
Marketing category: OTC MONOGRAPH FINAL
Marketing start: 2014-01-30
Marketing end: 0000-00-00
Substance: DEXTROMETHORPHAN HYDROBROMIDE
Active strength: 30 mg/10mL
NDC exclude flag: No
Listing certified through: 2021-12-31
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 · 2 matching rows.

Dataset, Scope, Product NDC table
Dataset	Scope	Product NDC	Package NDC	Code	Status	Reporting period	Source date
excluded product	product	76206-002		I	Inactivated by FDA		2026-09-09
excluded package	package	76206-002	76206-002-01	I	Inactivated by FDA		2026-09-09

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 · 38 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	76206-002-01	`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	76206-002-01	`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	76206-002-01	`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	76206-002-01	`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	76206-002-01	`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	76206-002-01	`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	76206-002-01	`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	76206-002-01	`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	76206-002-01	`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	76206-002-01	`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	76206-002-01	`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	76206-002-01	`557ba5c1ecfa…`	`9c80585c8c6e…`
2024-05-28 21:12 UTC · source 2024-05-28	excluded product	product		`8af77b9d5b6f…`	`d9bbb34c5368…`
2024-05-28 21:12 UTC · source 2024-05-28	excluded package	package	76206-002-01	`8af77b9d5b6f…`	`d9bbb34c5368…`
2024-05-15 03:39 UTC · source 2024-05-14	excluded product	product		`834df4deac94…`	`adcc014656a3…`
2024-05-15 03:39 UTC · source 2024-05-14	excluded package	package	76206-002-01	`834df4deac94…`	`adcc014656a3…`
2024-03-11 06:39 UTC · source 2024-03-08	excluded product	product		`1332a3947898…`	`d4bfe170f9cd…`
2024-03-11 06:39 UTC · source 2024-03-08	excluded package	package	76206-002-01	`1332a3947898…`	`d4bfe170f9cd…`
2022-08-30 03:57 UTC · source 2022-08-29	excluded product	product		`fb8cb913e6d1…`	`eb8c232b6be0…`
2022-08-30 03:57 UTC · source 2022-08-29	excluded package	package	76206-002-01	`fb8cb913e6d1…`	`eb8c232b6be0…`
2022-04-09 23:13 UTC · source 2022-04-08	excluded product	product		`86f5da6cb304…`	`a595104c45d7…`
2022-04-09 23:13 UTC · source 2022-04-08	excluded package	package	76206-002-01	`86f5da6cb304…`	`a595104c45d7…`
2022-04-04 05:40 UTC · source 2022-04-01	excluded product	product		`bd6a592717d7…`	`303034d00443…`
2022-04-04 05:40 UTC · source 2022-04-01	excluded package	package	76206-002-01	`bd6a592717d7…`	`303034d00443…`
2019-12-08 06:16 UTC · source 2019-12-05	excluded product	product		`110d247fa046…`	`a55b01930146…`
2019-12-08 06:16 UTC · source 2019-12-05	excluded package	package	76206-002-01	`110d247fa046…`	`a55b01930146…`

DailyMed Product Concepts#

Product concept, Relation, Version table
Product concept	Relation	Version	Effective
bf324df6-7127-7deb-def5-2681c136cd03	Product name	3	20250325
43a1ed49-eae2-4840-8075-cb4b33478540	Product name	1	20230425
ba088a92-ab5e-b2d4-e908-f5ea691b7587	Product name	7	20210201
76633df9-0d59-4b88-03ed-21dee1b966f8	Product name	1	20140508

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
76206-002-01	2022-01-28	C162847	48780-1	9855e2a2-4377-60a7-e053-dbdaa90a05bd	Drug Facts
76206-002-01	2020-06-02	C162847	48780-1	9855e2a2-4377-60a7-e053-dbdaa90a05bd	Drug Facts
76206-002-01	2019-11-27	C162847	48780-1	9855e2a2-4377-60a7-e053-dbdaa90a05bd	Drug Facts

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
76206-002-01	COUGH MEDICINEsoothing relief	6 in 1 BOX	LIQUID	6		3
76206-002-10	COUGH MEDICINEsoothing relief	10 mL in 1 BOTTLE, GLASS	LIQUID	10		3

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	DailyMed label	SPL version
DEXTROMETHORPHAN HYDROBROMIDE	ACTIVE INGREDIENT	9D2RTI9KYH	COUGH MEDICINE SOOTHING RELIEF (DEXTROMETHORPHAN) LIQUID [RFX PHARMACEUTICAL CO., LTD.]	1
DEXTROMETHORPHAN	ACTIVE MOIETY	7355X3ROTS	COUGH MEDICINE SOOTHING RELIEF (DEXTROMETHORPHAN) LIQUID [RFX PHARMACEUTICAL CO., LTD.]	1
APRICOT KERNEL OIL	INACTIVE INGREDIENT	54JB35T06A	COUGH MEDICINE SOOTHING RELIEF (DEXTROMETHORPHAN) LIQUID [RFX PHARMACEUTICAL CO., LTD.]	1
FRITILLARIA DELAVAYI BULB	INACTIVE INGREDIENT	AG6Q756AT7	COUGH MEDICINE SOOTHING RELIEF (DEXTROMETHORPHAN) LIQUID [RFX PHARMACEUTICAL CO., LTD.]	1
HONEY	INACTIVE INGREDIENT	Y9H1V576FH	COUGH MEDICINE SOOTHING RELIEF (DEXTROMETHORPHAN) LIQUID [RFX PHARMACEUTICAL CO., LTD.]	1
WATER	INACTIVE INGREDIENT	059QF0KO0R	COUGH MEDICINE SOOTHING RELIEF (DEXTROMETHORPHAN) LIQUID [RFX PHARMACEUTICAL CO., LTD.]	1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
76206-002	COUGH MEDICINE SOOTHING RELIEF (DEXTROMETHORPHAN) LIQUID [RFX PHARMACEUTICAL CO., LTD.]	3	Legacy NDC, 2 package rows	20200530_0de33537-117c-4ed4-a029-5432ebdf02ea.zip

UNII, Preferred term, Registry number table
UNII	Preferred term	Registry number	Matched term
9D2RTI9KYH	DEXTROMETHORPHAN HYDROBROMIDE	6700-34-1	DEXTROMETHORPHAN HYDROBROMIDE
7355X3ROTS	DEXTROMETHORPHAN	125-71-3	Dextromethorphan

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	DailyMed	SPL version
1090496	dextromethorphan HBr 15 MG in 5 mL Oral Solution	PSN	0de33537-117c-4ed4-a029-5432ebdf02ea	3
1090496	dextromethorphan hydrobromide 3 MG/ML Oral Solution	SCD	0de33537-117c-4ed4-a029-5432ebdf02ea	3
1090496	dextromethorphan hydrobromide 15 MG per 5 ML Oral Solution	SY	0de33537-117c-4ed4-a029-5432ebdf02ea	3
1090496	dextromethorphan hydrobromide 30 MG per 10 ML Oral Solution	SY	0de33537-117c-4ed4-a029-5432ebdf02ea	3

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
76206-002-01	76206000201	6 BOTTLE, GLASS in 1 BOX (76206-002-01) > 10 mL in 1 BOTTLE, GLASS (76206-002-10)		2014-01-30	0000-00-00	No	No	Current
76206-002-10	76206000210	10 mL in 1 BOTTLE, GLASS	10 ml					Historical