NDC 76206-005-05 - Soothe Comfort II Cough Syrup Herbal Mint

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
76206-005
Requested NDC
76206-005-05
Package NDCs from labels
76206-005-05, 76206-005-01
Manufacturer
RFX Pharmaceutical Co., Ltd.
Effective date
2021-04-28
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
Soothe Comfort II Cough Syrup Herbal Mint - RFX Pharmaceutical Co., Ltd.RFX Pharmaceutical Co., Ltd.2021-04-28HUMAN OTC DRUG LABEL

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
76206-005-012022-07-29C16284748780-1e4f33bdf-a009-d8a0-e053-dadaa90a6e4eRFXLMSootheComfortIICghSyrp

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
76206-005-01Soothe Comfort II Cough SyrupHerbal Mint1 in 1 BOXLIQUID11
76206-005-05Soothe Comfort II Cough SyrupHerbal Mint155 mL in 1 BOTTLE, GLASSLIQUID1551

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
76206-005SOOTHE COMFORT II COUGH SYRUP HERBAL MINT (DEXTROMETHORPHAN) LIQUID [RFX PHARMACEUTICAL CO., LTD.]1Legacy NDC, 2 package rows20210429_c10b5649-c79a-7805-e053-2a95a90ae865.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 11 of 11 · 201 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Eagle Brand Medicated Roll On RefreshCAMPHOR, MENTHOLBorden Company (Private) Limited567b6820-fb52-630e-e063-6294a90a8bf82015-07-01WarningsExact identifier
unii: AV092KU4JH

Reported adverse events (FAERS/openFDA)#

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