MGC Health

Product NDC: 83173-116
11-digit product format: 831730116
Labeler code: 83173
Product ID: 83173-116_3de65503-47d3-33ad-e063-6394a90ad2b2
Type: HUMAN OTC DRUG
Nonproprietary name: Cough Drops Assorted Citrus Vitamin C
Dosage form: TABLET, CHEWABLE, EXTENDED RELEASE
Route: ORAL
Labeler: Medical Group Care LLC
Application: M012
Marketing category: OTC MONOGRAPH DRUG
Marketing start: 2023-02-12
Substance: MENTHOL
Active strength: 2.7 mg/2850mg
NDC exclude flag: No
Listing certified through: 2026-12-31
Current FDA listing: Yes

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 · 16 matching rows.

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

Captured / source date, Dataset, Scope table
Captured / source date	Dataset	Scope	Package NDC	Code	Status	Snapshot	Source SHA-256
2025-08-27 00:01 UTC · source 2025-08-26	excluded product	product		I	Inactivated by FDA	`f5e01cc5f278…`	`a2eaf40c39c3…`
2025-08-27 00:01 UTC · source 2025-08-26	excluded package	package	83173-116-80	I	Inactivated by FDA	`f5e01cc5f278…`	`a2eaf40c39c3…`
2025-04-01 02:39 UTC · source 2025-03-31	excluded product	product		I	Inactivated by FDA	`2ef7874e63bc…`	`57b86245f4fa…`
2025-04-01 02:39 UTC · source 2025-03-31	excluded package	package	83173-116-80	I	Inactivated by FDA	`2ef7874e63bc…`	`57b86245f4fa…`
2025-03-28 20:22 UTC · source 2025-03-28	excluded product	product		I	Inactivated by FDA	`a1b67e2a42f9…`	`c4cf2c586c0d…`
2025-03-28 20:22 UTC · source 2025-03-28	excluded package	package	83173-116-80	I	Inactivated by FDA	`a1b67e2a42f9…`	`c4cf2c586c0d…`
2025-03-22 03:12 UTC · source 2025-03-21	excluded product	product		I	Inactivated by FDA	`cfe11265f3b6…`	`090c488252e2…`
2025-03-22 03:12 UTC · source 2025-03-21	excluded package	package	83173-116-80	I	Inactivated by FDA	`cfe11265f3b6…`	`090c488252e2…`
2025-03-10 12:48 UTC · source 2025-03-10	excluded product	product		I	Inactivated by FDA	`cdf11ea48f46…`	`ba0047e9e063…`
2025-03-10 12:48 UTC · source 2025-03-10	excluded package	package	83173-116-80	I	Inactivated by FDA	`cdf11ea48f46…`	`ba0047e9e063…`
2025-02-02 03:52 UTC · source 2025-01-31	excluded product	product		U	Excluded because listing certification expired	`302b2466d912…`	`e7b80fea0513…`
2025-02-02 03:52 UTC · source 2025-01-31	excluded package	package	83173-116-80	U	Excluded because listing certification expired	`302b2466d912…`	`e7b80fea0513…`
2025-01-20 13:05 UTC · source 2025-01-20	excluded product	product		U	Excluded because listing certification expired	`ed331223b511…`	`672a5bd82f5f…`
2025-01-20 13:05 UTC · source 2025-01-20	excluded package	package	83173-116-80	U	Excluded because listing certification expired	`ed331223b511…`	`672a5bd82f5f…`
2025-01-11 03:41 UTC · source 2025-01-10	excluded product	product		U	Excluded because listing certification expired	`0efc9e666f02…`	`f202fb6c5f17…`
2025-01-11 03:41 UTC · source 2025-01-10	excluded package	package	83173-116-80	U	Excluded because listing certification expired	`0efc9e666f02…`	`f202fb6c5f17…`

Reported adverse events (FAERS/openFDA)#

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

Additional Listing Data#

Finished product: Yes
Brand name base: MGC Health
Listing expiration: 2026-12-31

Active Ingredients#

Ingredient, Strength table
Ingredient	Strength
MENTHOL	2.7 mg/2850mg

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
L7T10EIP3A	Internal UNII lookup

Harmonized SPL set identifiers#

SPL set identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
f4a9cfec-0725-8f4a-e053-2995a90a1b4a	Available on FDA.report

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
83173-116-80	2025-09-03	C162847	48780-1	2cef2736-5f27-d83d-e063-dadaa90ab31f	MGC-YNBY Assorted Citrus Drops 80
83173-116-80	2025-01-30	C162847	48780-1	2cef2736-5f27-d83d-e063-dadaa90ab31f	MGC-YNBY Assorted Citrus Drops 80

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
83173-116-80	MGC Health	80 in 1 BAG	TABLET, CHEWABLE, EXTENDED RELEA	80		3
83173-116-80	MGC Health	2.7 mg in 1 DOSE PACK	TABLET, CHEWABLE, EXTENDED RELEA	2.7		3

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
83173-116	MGC HEALTH (COUGH DROPS ASSORTED CITRUS VITAMIN C) TABLET, CHEWABLE, EXTENDED RELEASE [MEDICAL GROUP CARE LLC]	2	Current NDC, 2 package rows	20230227_f4a9cfec-0725-8f4a-e053-2995a90a1b4a.zip

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 94 of 180 · 3,583 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Maximum Strength Mucus Relief DM	DEXTROMETHORPHAN HYDROBROMIDE AND GUAIFENESIN	Wal-Mart Stores,Inc.,	a748d5ab-901c-47bb-8437-997542ecebfe	2025-10-28	Warnings	Exact identifier application number: M012
Nighttime Childrens Multi Symptoms Cold and Cough Multi-Symptom Relief	CHLORPHENIRAMINE MALEATE AND DEXTROMETHORPHAN HYDROBROMIDE	WAL-MART STORES,INC.	68a68574-0fcb-4569-be57-d9aee5f62bea	2025-10-28	Warnings	Exact identifier application number: M012
Maximum Strength Mucus Relief Severe Congestion and Cough	DEXTROMETHORPHAN HYDROBROMIDE, GUAIFENESIN, AND PHENYLEPHRINE HYDROCHLORIDE	Wal-Mart Stores,Inc.,	635009a1-6154-4c62-a4be-d4f32c2cef8d	2025-10-28	Warnings	Exact identifier application number: M012
Publix Maximum Strength	OXYMETAZOLINE HYDROCHLORIDE	PUBLIX SUPER MARKETS, INC	cf49a06d-f095-48bf-bcd2-a410066ff9af	2025-10-28	Warnings	Exact identifier application number: M012
Publix	OXYMETAZOLINE HYDROCHLORIDE	PUBLIX SUPER MARKETS, INC	283e42b9-173c-4deb-9377-ff649efc177f	2025-10-28	Warnings	Exact identifier application number: M012
Publix Extra Moisturizing	OXYMETAZOLINE HYDROCHLORIDE	PUBLIX SUPER MARKETS, INC	eae83b75-9d5a-4100-9304-629e54ef7752	2025-10-28	Warnings	Exact identifier application number: M012
Publix	PHENYLEPHRINE HYDROCHLORIDE	PUBLIX SUPER MARKETS, INC	f10e120d-f0b7-4c51-b29b-e8cdbb1456f3	2025-10-28	Warnings	Exact identifier application number: M012
Family Care Nasal Relief	OXYMETAZOLINE HYDROCHLORIDE	United Exchange Corp	6d0f8e9e-0503-522b-e053-2a91aa0aca35	2025-10-28	Warnings	Exact identifier application number: M012
Family Care Nasal Relief	OXYMETAZOLINE HYDROCHLORIDE	United Exchange Corp	6d0eef2f-f546-d769-e053-2991aa0a8fe4	2025-10-28	Warnings	Exact identifier application number: M012
Sinus Plus Headache	ACETAMINOPHEN, PHENYLEPHRINE HCL	Kroger Company	b622b6cb-f756-439e-8684-d45ee1ea75ab	2025-10-28	Warnings	Exact identifier application number: M012
Tussin DM Cough and Chest Congestion Adult	DEXTROMETHORPHAN HBR, GUAIFENESIN	P & L Development, LLC	4af67ba7-8892-442c-b9fb-80aba9140e05	2025-10-28	Warnings	Exact identifier application number: M012
No Drip Nasal Mist Nasal Decongestant Severe Congestion	OXYMETAZOLINE HYDROCHLORIDE	Wal-Mart Stores,Inc.,	994fa270-65bb-4097-b88a-d5ce3c0e1c79	2025-10-27	Warnings	Exact identifier application number: M012
Dye Free Childrens Allergy Relief	DIPHENHYDRAMINE HYDROCHLORIDE	WAL-MART STORES INC.	3652ee94-b762-4100-a305-5acbec5f795a	2025-10-27	Warnings	Exact identifier application number: M012
Maximum Strength Mucus Relief Cold,Flu and Sore Throat	ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, GUAIFENESIN ,PHENYLEPHRINE HCL	Wal-Mart Stores,Inc.,	2fd5be4f-2bb6-4241-9e0f-be7610ae2fdc	2025-10-27	Warnings	Exact identifier application number: M012
Allergy Relief	DIPHENHYDRAMINE HCL	United Natural Foods, Inc. dba UNFI	4517c7ef-156c-42b8-a2da-165e936f0837	2025-10-27	Warnings	Exact identifier application number: M012
Allergies MY CHILD NEEDS HELP WITH	DIPHENHYDRAMINE HCL	Unconditional Love	5ad293e9-0a4b-4923-8a91-f01450726828	2025-10-27	Warnings	Exact identifier application number: M012
Allergy Relief	DIPHENHYDRAMINE HCL	Cardinal Health 110, LLC. DBA Leader	933a54d3-196d-4c5d-b26f-d18b2d2ba1df	2025-10-27	Warnings	Exact identifier application number: M012
Banophen	DIPHENHYDRAMINE HCL	Major Pharmaceuticals	69b7f7ca-7a3a-4fe6-a9bb-90b0e6ad62c1	2025-10-27	Warnings	Exact identifier application number: M012
basic care daytime severe cold and flu nighttime severe cold and flu	ACETAMINOPHEN, DEXTROMETHORPHAN HBR, DOXYLAMINE SUCCINATE, GUAIFENESIN, PHENYLEPHRINE HCL	Amazon.com Services LLC	4a9fd615-b7d3-452c-ac40-d9189124faaa	2025-10-24	Warnings	Exact identifier application number: M012
allergy childrens	DIPHENHYDRAMINE HYDROCHLORIDE	Meijer Distribution Inc	622b12fa-455c-4432-a9a2-698a929bbd68	2025-10-24	Warnings	Exact identifier application number: M012

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Sample	Exclude flag	Status
83173-116-80	83173011680	80 DOSE PACK in 1 BAG (83173-116-80) / 2.7 mg in 1 DOSE PACK	80 dose pack	2023-02-12	No	No	Current