FDA.reportPublic FDA data

INNER REFRESHING WASH

Manufacturer
MISMIZBio Inc.
Effective date
2018-03-17
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 22:54:56

Label at a glance#

ProductINNER REFRESHING WASH
Label structure1 sections

Label contents#

Full prescribing information#

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

INNER REFRESHING WASHINNER REFRESHING WASH

DOSAGE & ADMINISTRATION SECTION

OTC - WHEN USING SECTION

OTC - STOP USE SECTION

OTC - PURPOSE SECTION

OTC - PREGNANCY OR BREAST FEEDING SECTION

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

OTC - DO NOT USE SECTION

OTC - ACTIVE INGREDIENT SECTION

INACTIVE INGREDIENT SECTION

WARNINGS SECTION

INDICATIONS & USAGE SECTION

OTC - ASK DOCTOR SECTION

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
f52be47f-7aa7-46c0-b1fa-50c18dd50206Product name120201029
2ee8a2ab-68f9-45f5-8e16-b382e1af7d34Product name120200618
444b3e50-f226-46ef-bfca-2e7035d140cdProduct name120190611
7cda52fc-125f-421c-8fea-bc1974370c49Product name220180703
597b1cfd-7b31-5048-62be-ca5cd740da2fProduct name120140508
ec2149b3-5c6d-5344-f757-c86411073075Product name120140508

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
71984-3500-12022-01-28C16284748780-1d6a99b39-4ecc-a426-e053-dadaa90af4c267a882d2-8f08-711a-e053-2a91aa0a7f1d

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
71984-3500-1INNER REFRESHING WASH3 in 1 BOXSOLUTION31
71984-3500-1INNER REFRESHING WASH35 mL in 1 APPLICATORSOLUTION351

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
71984-3500INNER REFRESHING WASH (GLYCERIN) SOLUTION [MISMIZBIO INC.]12 package rows20180320_67a882d2-8f08-711a-e053-2a91aa0a7f1d.zip

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 23 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
71984-350071984-3500-1

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 22 matching rows.

Name, UNII, Kind table
NameUNIIKind
PENTYLENE GLYCOL50C1307PZGINGR
SCUTELLARIA BAICALENSIS ROOT7J95K7ID2SINGR
ROSA CENTIFOLIA FLOWERCS4TE8FF7OINGR
GLYCYRRHIZINATE DIPOTASSIUMCA2Y0FE3FXINGR
HYDROXYETHYL CELLULOSE (100 MPA.S AT 2%)R33S7TK2EPINGR
USNEA BARBATAD6DVA9TCAPINGR
GLYCYRRHIZA GLABRA2788Z9758HINGR
PUNICA GRANATUM WHOLEO2ZTS50U5EINGR
LACTITOLL2B0WJF7ZYINGR
BUTYLENE GLYCOL3XUS85K0RAINGR
COPTIS CHINENSIS ROOTCXS4LJR7ELINGR
MAGNOLIA KOBUS BARK54LVP49595INGR
HYALURONIC ACIDS270N0TRQYINGR
WATER059QF0KO0RINGR
PROPANEDIOL5965N8W85TINGR
SOYBEAN GERMJBW2VHD14MINGR
LACTIC ACID33X04XA5ATINGR
CENTELLA ASIATICA7M867G6T1UINGR
ZANTHOXYLUM PIPERITUM WHOLEY8IKP41338INGR
PULSATILLA KOREANA WHOLE5R35881OBKINGR
PAEONIA SUFFRUTICOSA ROOT7M7E9A2C8JINGR
GLYCERINPDC6A3C0OXINGR

Source Document#

Source XML

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 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
67a882d2-8f09-711a-e053-2a91aa0a7f1d67a882d2-8f08-711a-e053-2a91aa0a7f1d2018-03-17Exact identifier
spl id: 67a882d2-8f09-711a-e053-2a91aa0a7f1d
spl set id: 67a882d2-8f08-711a-e053-2a91aa0a7f1d

Reported adverse events (FAERS/openFDA)#

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