MEDIQUE Medikoff Drops

Product NDC: 47682-050
11-digit product format: 476820050
Labeler code: 47682
Product ID: 47682-050_3e4cb58c-fe20-ca13-e063-6394a90a7244
Type: HUMAN OTC DRUG
Nonproprietary name: MENTHOL
Dosage form: LOZENGE
Route: ORAL
Labeler: Unifirst First Aid Corporation
Application: M012
Marketing category: OTC MONOGRAPH DRUG
Marketing start: 2008-12-30
Substance: MENTHOL
Active strength: 7.6 mg/1
NDC exclude flag: No
Listing certified through: 2026-12-31
Current FDA listing: Yes

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: MEDIQUE Medikoff Drops
Listing expiration: 2026-12-31

Active Ingredients#

Ingredient, Strength table
Ingredient	Strength
MENTHOL	7.6 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
359751	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
0d6b4443-16a1-4851-bb03-d7407167551d	Available on FDA.report

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	SPL version
47682-050-22	MEDIQUE Medikoff Drops	75 in 1 BOX	LOZENGE	75	14
47682-050-60	MEDIQUE Medikoff Drops	600 in 1 BOX	LOZENGE	600	14
47682-050-64	MEDIQUE Medikoff Drops	24 in 1 BOX	LOZENGE	24	14
47682-050-66	MEDIQUE Medikoff Drops	601 in 1 BOX	LOZENGE	601	14
47682-050-69	MEDIQUE Medikoff Drops	6 in 1 BOX	LOZENGE	6	14

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDC	Billing unit	Product NDC	DailyMed indexing SPL	SPL version	Effective
47682-050-22	EA - Each	47682-050	c22f8e6e-44cd-477a-8a0c-ca5ff1268f7c	1	2012-07-24
47682-050-60	EA - Each	47682-050	e5229762-fb01-4452-8705-0d107c26c978	1	2012-07-24
47682-050-64	EA - Each	47682-050	6d39e7f9-82ca-4706-9a92-8784020e7f92	1	2012-07-24
47682-050-69	EA - Each	47682-050	8762556f-fe53-4815-866f-3bd92d669eb8	1	2012-07-24

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	DailyMed label	SPL version
MENTHOL	ACTIVE INGREDIENT	L7T10EIP3A	MEDIQUE MEDIKOFF DROPS (MENTHOL) LOZENGE MEDI-FIRST CHERRY COUGH DROPS (MENTHOL) LOZENGE MEDI FIRST PLUS CHERRY COUGH DROPS (MENTHOL) LOZENGE [UNIFIRST FIRST AID CORPORATION]	2
MENTHOL	ACTIVE MOIETY	L7T10EIP3A	MEDIQUE MEDIKOFF DROPS (MENTHOL) LOZENGE MEDI-FIRST CHERRY COUGH DROPS (MENTHOL) LOZENGE MEDI FIRST PLUS CHERRY COUGH DROPS (MENTHOL) LOZENGE [UNIFIRST FIRST AID CORPORATION]	2
CORN SYRUP	INACTIVE INGREDIENT	9G5L16BK6N	MEDIQUE MEDIKOFF DROPS (MENTHOL) LOZENGE MEDI-FIRST CHERRY COUGH DROPS (MENTHOL) LOZENGE MEDI FIRST PLUS CHERRY COUGH DROPS (MENTHOL) LOZENGE [UNIFIRST FIRST AID CORPORATION]	2
EUCALYPTUS OIL	INACTIVE INGREDIENT	2R04ONI662	MEDIQUE MEDIKOFF DROPS (MENTHOL) LOZENGE MEDI-FIRST CHERRY COUGH DROPS (MENTHOL) LOZENGE MEDI FIRST PLUS CHERRY COUGH DROPS (MENTHOL) LOZENGE [UNIFIRST FIRST AID CORPORATION]	2
FD&C RED NO. 40	INACTIVE INGREDIENT	WZB9127XOA	MEDIQUE MEDIKOFF DROPS (MENTHOL) LOZENGE MEDI-FIRST CHERRY COUGH DROPS (MENTHOL) LOZENGE MEDI FIRST PLUS CHERRY COUGH DROPS (MENTHOL) LOZENGE [UNIFIRST FIRST AID CORPORATION]	2
SUCROSE	INACTIVE INGREDIENT	C151H8M554	MEDIQUE MEDIKOFF DROPS (MENTHOL) LOZENGE MEDI-FIRST CHERRY COUGH DROPS (MENTHOL) LOZENGE MEDI FIRST PLUS CHERRY COUGH DROPS (MENTHOL) LOZENGE [UNIFIRST FIRST AID CORPORATION]	2

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
47682-050	MEDIQUE MEDIKOFF DROPS (MENTHOL) LOZENGE MEDI-FIRST CHERRY COUGH DROPS (MENTHOL) LOZENGE MEDI FIRST PLUS CHERRY COUGH DROPS (MENTHOL) LOZENGE [UNIFIRST FIRST AID CORPORATION]	13	Current NDC, Legacy NDC, 5 package rows	20241120_0d6b4443-16a1-4851-bb03-d7407167551d.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 115 of 180 · 3,583 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Benadryl	DIPHENHYDRAMINE HYDROCHLORIDE	Morning Star OTC	f4ff84b3-bb0c-4900-8ba4-6d1b90394782	2025-06-09	Warnings	Exact identifier application number: M012
Equate Kids Daytime Dex Cough Gels	DEXTROMETHORPHAN	Walmart	37269cd6-1528-9879-e063-6394a90a2b54	2025-06-09	Warnings	Exact identifier application number: M012
Nuvicare DayTime Cold and Flu Softgel	ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, PHENYLEPHRINE HYDROCHLORIDE	NUVICARE LLC	bdc35570-c8df-4797-a13e-7f2479ec42b7	2025-06-09	Warnings	Exact identifier application number: M012
Nuvicare DayTime and NightTime Cold and Flu	ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, PHENYLEPHRINE HYDROCHLORIDE, DOXYLAMINE SUCCINATE	NUVICARE LLC	f5764925-c586-40e4-8252-24d92389af01	2025-06-09	Warnings	Exact identifier application number: M012
Nuvicare NightTime Cold and Flu Softgel	ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, DOXYLAMINE SUCCINATE	NUVICARE LLC	2a29f0ed-d86b-4787-84e0-f7a8c5e7581f	2025-06-09	Warnings	Exact identifier application number: M012
Nuvicare DayTime and NightTime Cold and Flu	ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, PHENYLEPHRINE HYDROCHLORIDE, DOXYLAMINE SUCCINATE	NUVICARE LLC	7fa8e4ad-95cb-4905-90db-d53b3bc87c41	2025-06-09	Warnings	Exact identifier application number: M012
Vaporizing Steam Liquid	MEDICATED COUGH SUPPRESSANT	NeilMed Pharmaceuticals Inc.	36cf6218-adb8-9d8b-e063-6394a90a49a0	2025-06-05	Warnings	Exact identifier application number: M012
Geri-Tussin DM	DEXTROMETHORPHAN HBR, GUAIFENESIN	Geri-Care Pharmaceuticals, Corp	7e2fb43c-a7f1-4c1d-a700-7c6510999c03	2025-06-05	Warnings	Exact identifier application number: M012
CHILDRENS ROBITUSSIN COUGH AND COLD LONG-ACTING	CHLORPHENIRAMINE MALEATE, DEXTROMETRORPHAN HBR	Haleon US Holdings LLC	becb4025-b63e-f2ea-9d11-d51fdf4e5c13	2025-06-04	Warnings	Exact identifier application number: M012
Diphenhydramine HCL STRAWBERRY FLAVOR	DIPHENHYDRAMINE HCL	Innovida Pharmaeutique Corporation	7eb709a5-c587-4f1d-bc2d-576d07a3a3bf	2025-06-04	Warnings	Exact identifier application number: M012
Children Allergy Relief Bubblegum flavor	DIPHENHYDRAMINE HCL	TARGET CORPORATION	69d33f77-06e1-48fa-a516-892fdf11bb1c	2025-06-03	Warnings	Exact identifier application number: M012
oxymetazoline hydrochloride	OXYMETAZOLINE HYDROCHLORIDE	NuCare Pharmaceuticals,Inc.	fd058e2b-5445-e416-e053-6394a90a611b	2025-06-03	Warnings	Exact identifier application number: M012
Major Nasal Decongestant	OXYMETAZOLINE HYDROCHLORIDE	NuCare Pharmaceuticals, Inc.	36b1a7e0-c8b9-0890-e063-6394a90ab13a	2025-06-03	Warnings	Exact identifier application number: M012
COLD, FLU and SORE THROAT RELIEF	ACETAMINOPHEN 650 MG, DEXTROMETHORPHAN HBR 20 MG, GUAIFENESIN 400 MG, PHENYLEPHRINE HCL 10 MG	BETTER LIVING BRANDS, LLC	202d60a8-83da-5afc-e063-6394a90ad779	2025-05-31	Warnings	Exact identifier application number: M012
Allergy Relief	DIPHENHYDRAMINE HCL	TARGET CORPORATION	f935341f-1e33-d78e-e053-6294a90a348e	2025-05-30	Warnings	Exact identifier application number: M012
Diphenhydramine HCl	DIPHENHYDRAMINE HCL	AARNA USA INC.	365bb414-8425-a900-e063-6394a90aa887	2025-05-30	Warnings	Exact identifier application number: M012
Childrens Allergy	DIPHENHYDRAMINE HYDROCHLORIDE	P & L Development, LLC	8559be55-8b00-4353-8e26-b5dff2ada806	2025-05-30	Warnings	Exact identifier application number: M012
Daytime Nighttime Cold and Flu	ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, DOXYLAMINE SUCCINATE, PHENYLEPHRINE HYDROCHLORIDE	Walmart Inc.	35da8429-1f83-9e81-e063-6294a90a3515	2025-05-23	Warnings	Exact identifier application number: M012
MAXIMUM STRENGTH COLD AND FLU	ACETAMINOPHEN, DEXTROMETHORPHAN HBR, GUAIFENESIN, PHENYLEPHRINE HCL	TARGET CORP	9dfef3dc-dbc8-659a-e053-2995a90a8c3b	2025-05-21	Warnings	Exact identifier application number: M012
Adult Tussin	GUAIFENESIN	Camber Consumer Care	896d2540-279a-4405-b176-acbff56303e5	2025-05-20	Warnings	Exact identifier application number: M012

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	DailyMed	SPL version
359751	menthol 7.6 MG Oral Lozenge	PSN	0d6b4443-16a1-4851-bb03-d7407167551d	14
359751	menthol 7.6 MG Oral Lozenge	SCD	0d6b4443-16a1-4851-bb03-d7407167551d	14

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
47682-050-22	47682005022	75 LOZENGE in 1 BOX (47682-050-22)	75 lozenge	2008-12-30	0000-00-00	No	No	Current
47682-050-60	47682005060	600 LOZENGE in 1 BOX (47682-050-60)	600 lozenge	2008-12-30	0000-00-00	No	No	Current
47682-050-64	47682005064	24 LOZENGE in 1 BOX (47682-050-64)	24 lozenge	2008-12-30	0000-00-00	No	No	Current
47682-050-66	47682005066	601 LOZENGE in 1 BOX (47682-050-66)	601 lozenge	2008-12-30	0000-00-00	No	No	Current
47682-050-69	47682005069	6 LOZENGE in 1 BOX (47682-050-69)	6 lozenge	2008-12-30	0000-00-00	No	No	Current