FDA.reportPublic FDA data

Dr. YERMA INSTANT HAND SANITIZER

Manufacturer
MPRBRAIN CO.LTD
Effective date
2020-06-12
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:17:28

Label at a glance#

ProductDr. YERMA INSTANT HAND SANITIZER
Active ingredientALCOHOL
Label structure1 sections

Label contents#

Full prescribing information#

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Dr YERMA INSTANT HAND SANITIZER 300 mlDr YERMA INSTANT HAND SANITIZER 300 ml

OTC - ACTIVE INGREDIENT SECTION

DOSAGE & ADMINISTRATION SECTION

OTC - PURPOSE SECTION

INDICATIONS & USAGE SECTION

INACTIVE INGREDIENT SECTION

OTC - DO NOT USE SECTION

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

OTC - WHEN USING SECTION

INSTRUCTIONS FOR USE SECTION

WARNINGS SECTION

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
581662ethanol 70 % Topical GelPSN1
581662ethanol 0.7 ML/ML Topical GelSCD1
581662ethanol 70 % Topical GelSY1
581662ethyl alcohol 70 % Topical GelSY1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
74741-7301-12023-01-30C16284748780-1f386c64a-3b2c-0266-e053-dadaa90a7c1aDr. YERMA INSTANT HAND SANITIZER 300 ml : 74741-7301-1 (Bottle+Pump)

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
74741-7301-1Dr. YERMA INSTANT HAND SANITIZER300 mL in 1 BOTTLE, PUMPGEL3001

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
74741-7301DR. YERMA INSTANT HAND SANITIZER (ETHANOL) GEL [MPRBRAIN CO.LTD]1Legacy NDC, 1 package rows20200613_a7df4ecc-c956-dd2c-e053-2a95a90a9d50.zip

Products#

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

DailyMed product names page 1 of 1 · 20 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
74741-730174741-7301-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 18 matching rows.

Name, UNII, Kind table
NameUNIIKind
SOYBEAN GERMJBW2VHD14MIACT
DIPROPYLENE GLYCOLE107L85C40IACT
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE0A5MM307FCIACT
GREEN TEA LEAFW2ZU1RY8B0IACT
PEG-60 HYDROGENATED CASTOR OIL02NG325BQGIACT
BUTYLENE GLYCOL3XUS85K0RAIACT
WATER059QF0KO0RIACT
PROPYLENE GLYCOL6DC9Q167V3IACT
SCUTELLARIA BAICALENSIS ROOT7J95K7ID2SIACT
CHINESE CINNAMONWS4CQ062KMIACT
PURSLANEM6S840WXG5IACT
TROLAMINE9O3K93S3TKIACT
ALOE VERA LEAFZY81Z83H0XIACT
OREGANO0E5AT8T16UIACT
SALIX ALBA BARK205MXS71H7IACT
CHAMAECYPARIS OBTUSA LEAF7OL154J5XBIACT
1,2-HEXANEDIOLTR046Y3K1GIACT
ALCOHOL3K9958V90MACTIB

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
a7df201f-b784-5cf5-e053-2995a90a8cf6a7df4ecc-c956-dd2c-e053-2a95a90a9d502020-06-12Exact identifier
spl id: a7df201f-b784-5cf5-e053-2995a90a8cf6
spl set id: a7df4ecc-c956-dd2c-e053-2a95a90a9d50

Reported adverse events (FAERS/openFDA)#

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