Ludens

Product NDC: 52183-227
11-digit product format: 521830227
Labeler code: 52183
Product ID: 52183-227_596bafe3-fc62-46eb-e063-6294a90a9431
Type: HUMAN OTC DRUG
Nonproprietary name: pectin and menthol
Dosage form: LOZENGE
Route: ORAL
Labeler: Prestige Brands Holdings, Inc.
Application: M022
Marketing category: OTC MONOGRAPH DRUG
Marketing start: 2018-06-15
Marketing end: 2027-03-31
Substance: PECTIN; MENTHOL
Active strength: 2.8; 2.5 mg/1; mg/1
NDC exclude flag: No
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: Ludens
Brand name suffix: Dual Relief

Active Ingredients#

Ingredient, Strength table
Ingredient	Strength
PECTIN	2.8 mg/1
MENTHOL	2.5 mg/1

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 2 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
89NA02M4RX	Internal UNII lookup
L7T10EIP3A	Internal UNII lookup

Harmonized RxCUI identifiers#

RxCUI identifiers page 1 of 1 · 2 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
2056063	Internal RxNorm lookup
2056069	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
d0213cb3-ec8e-40cc-82c9-694032f0490f	Available on FDA.report

DailyMed Product Concepts#

Product concept, Relation, Version table
Product concept	Relation	Version	Effective
6bd95106-a412-1dad-b9cc-4cb74bfb27ce	Product name	2	20230315
baf7f49c-75b6-496b-a00e-8e766a8e4f03	Product name	1	20210127
ebc62596-fc97-4d03-9483-7ba095d25db7	Product name	1	20151210
d5e51f11-ad28-caa4-4b49-4143974782ad	Product name	1	20150831
290f523a-f9db-9774-b5a9-e1f908ac1782	Product name	1	20150828
0ca1d589-929b-4b33-bc5b-1d84abdafa6a	Product name	1	20150324
fc363c46-397b-4476-ac0f-70e43e8e4592	Product name	1	20150324
c6b65c52-69c7-df49-550a-a50c137f6218	Product name	1	20140508

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
52183-227-25	LudensDual Relief	25 in 1 BAG	LOZENGE	25		3

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
52183-227	LUDENS DUAL RELIEF (PECTIN AND MENTHOL) LOZENGE [PRESTIGE BRANDS HOLDINGS, INC.]	2	Current NDC, Legacy NDC, 1 package rows	20241113_d0213cb3-ec8e-40cc-82c9-694032f0490f.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 16 of 40 · 786 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
GuruNanda Oxyfusion	HYDROGEN PEROXIDE	GURUNANDA, LLC	3be317b9-a5d8-b198-e063-6394a90af985	2025-11-11	Warnings	Exact identifier application number: M022
GuruNanda Oral Pain Relief	MENTHOL	GURUNANDA, LLC	3b8f3562-0e46-bea4-e063-6294a90adb71	2025-11-11	Warnings	Exact identifier application number: M022
TopCare Cherry Flavor	PHENOL	TOPCO ASSOCIATES, LLC	5d3f0610-deb4-4180-ae19-2c65ed2f368b	2025-11-10	Warnings	Exact identifier application number: M022
Topcare Sore Throat Menthol Flavor	PHENOL	TOPCO ASSOCIATES LLC	fb1f2c11-2508-4985-bae5-7d547bd6aa23	2025-11-10	Warnings	Exact identifier application number: M022
Zilactin-B	BENZOCAINE	ASCENT CONSUMER PRODUCTS, INC	42eeb3d4-bac6-4e29-e063-6294a90a644d	2025-11-06	Warnings	Exact identifier application number: M022
Zilactin Early Relief Cold Sore	BENZYL ALCOHOL	ASCENT CONSUMER PRODUCTS, INC	42ef8bfa-c4d9-01cf-e063-6394a90ac88a	2025-11-06	Warnings	Exact identifier application number: M022
HurriCaine Topical Anesthetic Gel	BENZOCAINE	Beutlich Pharmaceuticals, LLC	106b6115-d043-4050-80c6-1d82456dea02	2025-11-06	Warnings	Exact identifier application number: M022
HurriCaine Topical Anesthetic Gel	BENZOCAINE	Beutlich Pharmaceuticals, LLC	4c278122-2643-46bf-9e44-11985210a16e	2025-11-06	Warnings	Exact identifier application number: M022
HurriCaine Topical Anesthetic Liquid	BENZOCAINE	Beutlich Pharmaceuticals, LLC	fee9969d-ad1a-4f44-9741-a0a44c9e1128	2025-11-06	Warnings	Exact identifier application number: M022
Ear Wax Removal Aid Drops	CARBAMIDE PEROXIDE	Target Corporation	0ddf9945-147d-4b25-98a6-4e9f12a4656f	2025-11-05	Warnings	Exact identifier application number: M022
Alpha-Caine Topical Anesthetic	BENZOCAINE	Dental Technologies, Inc.	e6a312e5-17ac-46f0-8723-4e40eeecd69f	2025-11-04	Warnings	Exact identifier application number: M022
PEROXY SHIELD MOUTH SORE	1.5% HYDROGEN PEROXIDE	Dental Technologies, Inc.	a72e433b-1b7d-4a0c-e053-2995a90a30c4	2025-11-04	Warnings	Exact identifier application number: M022
Alpha-Caine Topical Anesthetic	BENZOCAINE	Dental Technologies, Inc.	ae628766-25b7-4b4f-abb8-a43faf2f44b9	2025-11-04	Warnings	Exact identifier application number: M022
Alpha-Caine Topical Anesthetic	BENZOCAINE	Dental Technologies, Inc.	719743f9-21fc-4568-b879-acdfa4639464	2025-11-04	Warnings	Exact identifier application number: M022
Alpha-Caine Topical Anesthetic	BENZOCAINE	Dental Technologies, Inc.	ff0695a1-1d7d-4b51-97fd-689e56d914fe	2025-11-04	Warnings	Exact identifier application number: M022
Antiseptic	EUCALYPTOL, MENTHOL, METHYL SALICYLATE, THYMOL	Family Dollar (FAMILY WELLNESS)	f7edf75c-cdba-4dde-bfc5-a04af34759d3	2025-11-03	Warnings	Exact identifier application number: M022
7 Select Oral Pain Maximum Strength Relief	BENZOCAINE	7-ELEVEN, INC.	f170a570-1c50-4b9a-be16-9b01bf5eaa74	2025-10-31	Warnings	Exact identifier application number: M022
Oral Pain Relief	BENZOCAINE AND BENZALKONIUM CHLORIDE	Universal Distribution Center LLC	18520f9b-4d35-1e9c-e063-6294a90aaa39	2025-10-30	Warnings	Exact identifier application number: M022
Iodent Oral Analgesic	BENZOCAINE	United Exchange Corp.	63902125-f8dc-0ada-e053-2991aa0a7ce5	2025-10-30	Warnings	Exact identifier application number: M022
Ear Wax Removal Aid Drops	CARBAMIDE PEROXIDE	BETTER LIVING BRANDS, LLC	3bded237-4d2c-4b38-bedc-267fdc374194	2025-10-29	Warnings	Exact identifier application number: M022

UNII, Preferred term, Registry number table
UNII	Preferred term	Registry number	Matched term
89NA02M4RX	PECTIN	9000-69-5	PECTIN

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	DailyMed	SPL version
2056069	Luden's Dual Relief 2.5 MG / 2.8 MG Oral Lozenge	PSN	d0213cb3-ec8e-40cc-82c9-694032f0490f	3
2056063	menthol 2.5 MG / pectin 2.8 MG Oral Lozenge	PSN	d0213cb3-ec8e-40cc-82c9-694032f0490f	3
2056069	menthol 2.5 MG / pectin 2.8 MG Oral Lozenge [Luden's Dual Relief]	SBD	d0213cb3-ec8e-40cc-82c9-694032f0490f	3
2056063	menthol 2.5 MG / pectin 2.8 MG Oral Lozenge	SCD	d0213cb3-ec8e-40cc-82c9-694032f0490f	3
2056069	Luden's Dual Relief (menthol 2.5 MG / pectin 2.8) MG Oral Lozenge	SY	d0213cb3-ec8e-40cc-82c9-694032f0490f	3

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
52183-227-25	52183022725	25 LOZENGE in 1 BAG (52183-227-25)	25 lozenge	2018-06-15	2027-03-31	No	No	Current

Title, Manufacturer, Effective date table
Title	Manufacturer	Effective date	Type	Version
Ludens Dual Relief Wild Cherry - 52183-227-25	Prestige Brands Holdings, Inc.	2026-08-19	HUMAN OTC DRUG LABEL	4