NDC 66613-8459 - Rohto Dual Light Relief

This NDC is not currently matched to an FDA NDC product listing in FDA.report, but it is a valid NDC-form code. FDA.report is showing the available DailyMed label context for the product root.

Product NDC: 66613-8459
Package NDCs from labels: 66613-8459-1
Manufacturer: Rohto Pharmaceutical Co., Ltd. | The Mentholatum Company
Effective date: 2024-12-19
Current FDA listing: Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
Label	Manufacturer	Effective date	Type
CHLOROBUTANOL - Rohto Pharmaceutical Co., Ltd. \| The Mentholatum Company	Rohto Pharmaceutical Co., Ltd. \| The Mentholatum Company	2024-12-19	HUMAN OTC DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
66613-8459-1	RohtoDual Light Relief	1 in 1 CARTON	LIQUID	1		2
66613-8459-1	RohtoDual Light Relief	18 mL in 1 BOTTLE, DISPENSING	LIQUID	18		2

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
66613-8459	ROHTO DUAL LIGHT RELIEF (HYPROMELLOSE, POVIDONE) LIQUID [ROHTO PHARMACEUTICAL CO., LTD.]	2	2 package rows	20241222_1bbde83e-a64e-1a0f-e063-6394a90af4ff.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 50 of 50 · 983 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Eagle Brand Medicated Roll On Refresh	CAMPHOR, MENTHOL	Borden Company (Private) Limited	567b6820-fb52-630e-e063-6294a90a8bf8	2015-07-01	Warnings	Exact identifier unii: 5TJD82A1ET
Eagle Brand Medicated Oil Aromatic	CAMPHOR, MENTHOL, METHYL SALICYLATE	Borden Company (Private) Limited	54e45d89-e8c3-6fc3-e063-6394a90aac4e	2015-06-15	Warnings	Exact identifier unii: 5TJD82A1ET
CPDA-1	ANTICOAGULANT CITRATE PHOSPHATE DEXTROSE ADENINE	Fenwal, Inc.	051f7347-5a76-4664-8fe2-e61b3dfcb0e4	2014-08-27		Exact identifier unii: XF417D3PSL unii: B22547B95K

Reported adverse events (FAERS/openFDA)#

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