IMU

Manufacturer
RAPHAGEN CO. LTD
Effective date
2017-01-12
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 22:48:26

Label at a glance#

ProductIMU
Active ingredientLACTOBACILLUS HELVETICUS, RICE BRAN
Label structure8 sections

Label contents#

Full prescribing information#

ACTIVE INGREDIENT

OTC - ACTIVE INGREDIENT SECTION

Active Ingredient: LACTOBACILLUS HELVETICUS 1.00 % , RICE BRAN 1.00%

INACTIVE INGREDIENT

INACTIVE INGREDIENT SECTION

Inactive Ingredients: Water(Aqua), Glycerin, Cocamidopropyl Betaine, Decyl Glucoside, Alcohol, Propanediol, Paeonia Suffruticosa Root Extract, Allantoin, Centella Asiatica Extract, Sodium Chloride, Hydroxyacetophenone, PEG-60 Hydrogenated Castor Oil, Lactic Acid, Menthol, Disodium EDTA, Fragrance(Parfum)

PURPOSE

OTC - PURPOSE SECTION

Purpose: Sanitizer

WARNINGS

WARNINGS SECTION

Warnings: 1. In case of having following symptoms after using this product, stop using it immediately. If the symptoms get worse, you need to consult a dermatologist. 1) In case of having problems such as red spots, swelling, itching or irritation during using this product 2) In case of having the same symptoms above on the part where you put this product, which is exposed to direct sunlight. 2. Do not use it on the part where you have a scar, eczema or dermatitis. 3. Topical use only 4. Keep out of reach of children

KEEP OUT OF REACH OF CHILDREN

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

KEEP OUT OF REACH OF CHILDREN

INDICATIONS & USAGE

INDICATIONS & USAGE SECTION

Indications & usage: 1. Two or three times the pump out less on the palm of the press an adequate amount of foam. 2. Rub gently massage it in as along the external genitals and anal. 3. Rinse with tepid water well. 4. You can use every day. 1 day more than three times.

DOSAGE & ADMINISTRATION

DOSAGE & ADMINISTRATION SECTION

Dosage & Administration: Two or three times the pump out less on the palm of the press an adequate amount of foam.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Image of cartonImage of carton

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
BarcodeEAN-138809531460008GTIN-13: 8809531460008
EAN-13: 8809531460008
GTIN storage (14 digits): 08809531460008
imu carton.jpg

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
71125-010-022020-01-31C16284748780-19d75b9d0-7012-f424-e053-dadaa90a57ce568a9b73-d4e8-4596-8aa3-123382a6e4c9

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
71125-010-01IMU150 mL in 1 BOTTLE, PUMPAEROSOL, FOAM1501
71125-010-02IMU1 in 1 CARTONAEROSOL, FOAM11

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
71125-010IMU (LACTOBACILLUS HELVETICUS, RICE BRAN) AEROSOL, FOAM [RAPHAGEN CO. LTD]1Legacy NDC, 2 package rows20170112_568a9b73-d4e8-4596-8aa3-123382a6e4c9.zip

Products#

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

DailyMed product names page 1 of 1 · 6 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
71125-01071125-010-01, 71125-010-02

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 4 matching rows.

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
fe6b6c5f-0d9e-46f2-ac18-a676e2da96db568a9b73-d4e8-4596-8aa3-123382a6e4c92017-01-12WarningsExact identifier
spl id: fe6b6c5f-0d9e-46f2-ac18-a676e2da96db
spl set id: 568a9b73-d4e8-4596-8aa3-123382a6e4c9

Reported adverse events (FAERS/openFDA)#

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