Honey Lemon Cough Drops

Product NDC: 52642-044
11-digit product format: 526420044
Labeler code: 52642
Product ID: 52642-044_47465083-f501-0b05-e063-6394a90a02ee
Type: HUMAN OTC DRUG
Nonproprietary name: Menthol
Dosage form: LOZENGE
Route: ORAL
Labeler: Bestco Inc.
Application: M012
Marketing category: OTC MONOGRAPH DRUG
Marketing start: 2018-10-11
Substance: MENTHOL
Active strength: 7.5 mg/1
NDC exclude flag: No
Listing certified through: 2026-12-31
Current FDA listing: Yes

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	52642-044		D	Discontinued by firm		2026-10-21
excluded package	package	52642-044	52642-044-40	D	Discontinued by firm		2026-10-21

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 · 30 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
2025-12-14 17:58 UTC · source 2025-12-05	excluded product	product		D	Discontinued by firm	`d630ba8d3edf…`	`732f749b63fb…`
2025-12-14 17:58 UTC · source 2025-12-05	excluded package	package	52642-044-40	D	Discontinued by firm	`d630ba8d3edf…`	`732f749b63fb…`
2025-08-27 00:01 UTC · source 2025-08-26	excluded product	product		D	Discontinued by firm	`f5e01cc5f278…`	`a2eaf40c39c3…`
2025-08-27 00:01 UTC · source 2025-08-26	excluded package	package	52642-044-40	D	Discontinued by firm	`f5e01cc5f278…`	`a2eaf40c39c3…`
2025-04-01 02:39 UTC · source 2025-03-31	excluded product	product		D	Discontinued by firm	`2ef7874e63bc…`	`57b86245f4fa…`
2025-04-01 02:39 UTC · source 2025-03-31	excluded package	package	52642-044-40	D	Discontinued by firm	`2ef7874e63bc…`	`57b86245f4fa…`
2025-03-28 20:22 UTC · source 2025-03-28	excluded product	product		D	Discontinued by firm	`a1b67e2a42f9…`	`c4cf2c586c0d…`
2025-03-28 20:22 UTC · source 2025-03-28	excluded package	package	52642-044-40	D	Discontinued by firm	`a1b67e2a42f9…`	`c4cf2c586c0d…`
2025-03-22 03:12 UTC · source 2025-03-21	excluded product	product		D	Discontinued by firm	`cfe11265f3b6…`	`090c488252e2…`
2025-03-22 03:12 UTC · source 2025-03-21	excluded package	package	52642-044-40	D	Discontinued by firm	`cfe11265f3b6…`	`090c488252e2…`
2025-03-10 12:48 UTC · source 2025-03-10	excluded product	product		D	Discontinued by firm	`cdf11ea48f46…`	`ba0047e9e063…`
2025-03-10 12:48 UTC · source 2025-03-10	excluded package	package	52642-044-40	D	Discontinued by firm	`cdf11ea48f46…`	`ba0047e9e063…`
2025-02-02 03:52 UTC · source 2025-01-31	excluded product	product		D	Discontinued by firm	`302b2466d912…`	`e7b80fea0513…`
2025-02-02 03:52 UTC · source 2025-01-31	excluded package	package	52642-044-40	D	Discontinued by firm	`302b2466d912…`	`e7b80fea0513…`
2025-01-20 13:05 UTC · source 2025-01-20	excluded product	product		D	Discontinued by firm	`ed331223b511…`	`672a5bd82f5f…`
2025-01-20 13:05 UTC · source 2025-01-20	excluded package	package	52642-044-40	D	Discontinued by firm	`ed331223b511…`	`672a5bd82f5f…`
2025-01-11 03:41 UTC · source 2025-01-10	excluded product	product		D	Discontinued by firm	`0efc9e666f02…`	`f202fb6c5f17…`
2025-01-11 03:41 UTC · source 2025-01-10	excluded package	package	52642-044-40	D	Discontinued by firm	`0efc9e666f02…`	`f202fb6c5f17…`
2024-11-09 02:27 UTC · source 2024-11-08	excluded product	product		D	Discontinued by firm	`ad56d346431e…`	`cc804d4bbf1e…`
2024-11-09 02:27 UTC · source 2024-11-08	excluded package	package	52642-044-40	D	Discontinued by firm	`ad56d346431e…`	`cc804d4bbf1e…`
2024-10-04 04:10 UTC · source 2024-10-03	excluded product	product		D	Discontinued by firm	`367a005e9d99…`	`383a685ebd0f…`
2024-10-04 04:10 UTC · source 2024-10-03	excluded package	package	52642-044-40	D	Discontinued by firm	`367a005e9d99…`	`383a685ebd0f…`
2024-07-10 04:00 UTC · source 2024-07-09	excluded product	product		D	Discontinued by firm	`557ba5c1ecfa…`	`9c80585c8c6e…`
2024-07-10 04:00 UTC · source 2024-07-09	excluded package	package	52642-044-40	D	Discontinued by firm	`557ba5c1ecfa…`	`9c80585c8c6e…`
2022-08-30 03:57 UTC · source 2022-08-29	excluded product	product		I	Inactivated by FDA	`fb8cb913e6d1…`	`eb8c232b6be0…`
2022-08-30 03:57 UTC · source 2022-08-29	excluded package	package	52642-044-40	I	Inactivated by FDA	`fb8cb913e6d1…`	`eb8c232b6be0…`
2022-04-09 23:13 UTC · source 2022-04-08	excluded product	product		I	Inactivated by FDA	`86f5da6cb304…`	`a595104c45d7…`
2022-04-09 23:13 UTC · source 2022-04-08	excluded package	package	52642-044-40	I	Inactivated by FDA	`86f5da6cb304…`	`a595104c45d7…`
2022-04-04 05:40 UTC · source 2022-04-01	excluded product	product		I	Inactivated by FDA	`bd6a592717d7…`	`303034d00443…`
2022-04-04 05:40 UTC · source 2022-04-01	excluded package	package	52642-044-40	I	Inactivated by FDA	`bd6a592717d7…`	`303034d00443…`

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: Honey Lemon Cough Drops
Listing expiration: 2026-12-31

Active Ingredients#

Ingredient, Strength table
Ingredient	Strength
MENTHOL	7.5 mg/1

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 RxCUI identifiers#

RxCUI identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
1250189	Internal RxNorm lookup

Harmonized SPL set identifiers#

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

Identifier, FDA.report destination table
Identifier	FDA.report destination
77f89a64-f4a4-f909-e053-2a91aa0ad44d	Available on FDA.report

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
52642-044-40	2023-11-06	C162847	48780-1	d6a99b39-6b7a-a426-e053-dadaa90af4c2	Menthol 7.5 mg
52642-044-40	2022-01-28	C162847	48780-1	d6a99b39-6b7a-a426-e053-dadaa90af4c2	Menthol 7.5 mg

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
52642-044-30	Honey Lemon Cough Drops	30 in 1 BAG	LOZENGE	30		7
52642-044-80	Honey Lemon Cough Drops	80 in 1 BAG	LOZENGE	80		7

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
52642-044	HONEY LEMON COUGH DROPS (MENTHOL) LOZENGE [BESTCO INC.]	6	Current NDC, Legacy NDC, 1 package rows	20241202_77f65f59-7ea1-adce-e053-2991aa0a6f1f.zip
52642-044	HONEY LEMON COUGH DROPS (MENTHOL) LOZENGE [BESTCO INC.]	6	Current NDC, Legacy NDC, 1 package rows	20241202_77f89a64-f4a4-f909-e053-2a91aa0ad44d.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 120 of 178 · 3,551 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
AXIV DayTime	ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE	VIVUNT PHARMA LLC	131b1f17-cd86-f9b3-e063-6294a90a3028	2025-02-12	Warnings	Exact identifier application number: M012
Maximum Strength Mucus Relief DM Max	DEXTROMETHORPHAN HBR, GUAIFENESIN	Topco Associates, LLC	17d0dbc7-c8c2-7917-e063-6394a90a42af	2025-02-12	Warnings	Exact identifier application number: M012
DAYTIME COLD AND FLU	DEXTROMETHORPHAN HYDROBROMIDE, ACETAMINOPHEN, PHENYLEPHRINE HYDROCHLORIDE	Kroger Company	bc00bbf8-52bb-fa75-e053-2a95a90a9406	2025-02-11	Warnings	Exact identifier application number: M012
Daytime cold and flu	ACETAMINOPHEN, DEXTROMETHORPHAN HBR, PHENYLEPHRINE HCI 325, 10, 5 MG SOFTGELS	TIME CAP LABORATORIES, INC.	fd24653e-c4fa-3c09-e053-6394a90aaa9e	2025-02-10	Warnings	Exact identifier application number: M012
Daytime Nighttime Cold and Flu	ACETAMINOPHEN, DEXTROMETHORPHAN HBR, PHENYLEPHRINE HCI, DOXYLAMINE SUCCINATE 325, 10/15, 5, 6.25 MG SOFTGELS	TIME CAP LABORATORIES INC.	fd81dd4b-9617-f4c1-e053-6394a90a5e72	2025-02-10	Warnings	Exact identifier application number: M012
Allergy Relief	DIPHENHYDRAMINE HYDROCHLORIDE	DOLGENCORP, LLC	be2207b7-b8f8-7fba-e053-2a95a90abd16	2025-02-10	Warnings	Exact identifier application number: M012
NIGHTTIME COLD AND FLU	DEXTROMETHORPHAN HYDROBROMIDE, ACETAMINOPHEN, DOXYLAMINE SUCCINATE	Kroger Company	bc0115a3-5322-855d-e053-2995a90aba27	2025-02-10	Warnings	Exact identifier application number: M012
Day time high blood pressure cold and flu	ACETAMINOPHEN DEXTROMETHORPHAN HBR	Camber Consumer Care	09fbd872-0970-4864-9308-4a7b85983920	2025-02-10	Warnings	Exact identifier application number: M012
Cough Drops	MENTHOL	The Kroger CO	f05e11ce-c908-acbc-e053-2a95a90a584e	2025-02-09	Warnings	Exact identifier application number: M012
Cough Drops	MENTHOL	The Kroger CO	f035c499-cda6-fadf-e053-2995a90af457	2025-02-09	Warnings	Exact identifier application number: M012
Cough Drops	MENTHOL	The Kroger CO	f6d977ce-bbca-f1cc-e053-6394a90acc96	2025-02-09	Warnings	Exact identifier application number: M012
Cough Drops	MENTHOL	The Kroger CO	f6da36d3-496d-2336-e053-6394a90a0f83	2025-02-09	Warnings	Exact identifier application number: M012
Cough Drops	MENTHOL	The Kroger CO	f6da2e02-42c7-1ede-e053-6394a90aff5f	2025-02-09	Warnings	Exact identifier application number: M012
MUCOSA DM	GUAIFENESIN DEXTROMETHORPHAN	TIME CAP LABORATORIES, INC.	62c1f4aa-6571-414c-9a58-31e107b7db97	2025-02-08	Warnings	Exact identifier application number: M012
Childrens Cough and Chest Congestion	DEXTROMETHORPHAN HBR, GUAIFENESIN	Genexa Inc.	2d95d5a4-34dc-e195-e063-6394a90a39da	2025-02-07	Warnings	Exact identifier application number: M012
Halls Sugar Free Honey Lemon	MENTHOL	Mondelez Global LLC	5d56ccd2-1c28-4750-9454-44809091ad2f	2025-02-05	Warnings	Exact identifier application number: M012
SanaTos Mucus Relief Cold Toddlers	DEXTROMETHORPHAN HBR, GUAIFENESIN	Pharmadel LLC	60672feb-1421-651e-e053-2a91aa0af41d	2025-02-04	Warnings	Exact identifier application number: M012
SofSkin Vaporizing Chest Rub and Cough Suppressant	CAMPHOR, MENTHOL, EUCALYPTUS OIL	Viny Health and Beauty Inc	34626cf5-64fc-15c0-e063-6294a90aa310	2025-02-04	Warnings	Exact identifier application number: M012
Pain Reliever PM	ACETAMINOPHEN, DIPHENHYDRAMINE HCL	CVS PHARMACY, INC	17922df7-7867-4300-bd99-55aee7b60606	2025-02-04	Warnings	Exact identifier application number: M012
No Drip Nasal Mist	OXYMETAZOLINE SPRAY	CVS Health	f4b8ff54-47b5-4d18-bf4e-b101abb22a24	2025-02-03	Warnings	Exact identifier application number: M012

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	DailyMed	SPL version
1250189	menthol 7.5 MG Oral Lozenge	PSN	77f65f59-7ea1-adce-e053-2991aa0a6f1f	7
1250189	menthol 7.5 MG Oral Lozenge	PSN	77f89a64-f4a4-f909-e053-2a91aa0ad44d	7
1250189	menthol 7.5 MG Oral Lozenge	SCD	77f65f59-7ea1-adce-e053-2991aa0a6f1f	7
1250189	menthol 7.5 MG Oral Lozenge	SCD	77f89a64-f4a4-f909-e053-2a91aa0ad44d	7

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
52642-044-30	52642004430	30 LOZENGE in 1 BAG (52642-044-30)	30 lozenge	2018-10-11	0000-00-00	No	No	Current
52642-044-40	52642004440	40 LOZENGE in 1 BAG (52642-044-40)	40 lozenge	2018-10-11	0000-00-00	No	No	Current
52642-044-80	52642004480	80 LOZENGE in 1 BAG (52642-044-80)	80 lozenge	2018-10-11	0000-00-00	No	No	Current

Title, Manufacturer, Effective date table
Title	Manufacturer	Effective date	Type	Version
Menthol 7.5 mg	Bestco Inc.	2025-12-31	HUMAN OTC DRUG LABEL	7
Menthol 7.5 mg	Bestco Inc.	2025-12-31	HUMAN OTC DRUG LABEL	7
Menthol 7.5 mg	Bestco Inc.	2023-11-06	HUMAN OTC DRUG LABEL	3