FDA.reportPublic FDA data

QB Skin Lab Hand Sanitizer

Manufacturer
Quorum Bio Pharmaceutical Co., Ltd.
Effective date
2020-04-21
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:07:39

Label at a glance#

ProductQB Skin Lab Hand Sanitizer
Active ingredientALCOHOL
Label structure1 sections

Label contents#

Full prescribing information#

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

70 tube70 tube

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 Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
efd58dcf-540a-4531-8766-e713129ca6f2Product name120250307
0ca1d589-929b-4b33-bc5b-1d84abdafa6aProduct name120150324
fc363c46-397b-4476-ac0f-70e43e8e4592Product name120150324
1681bc73-b05f-12c3-1075-382ae39f449cProduct name120140508

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
75710-078-012023-01-30C16284748780-1f386c649-a54c-0266-e053-dadaa90a7c1aQB Skin Lab Hand Sanitizer 70 ml : 75710-078-01

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
75710-078-01QB Skin Lab Hand Sanitizer70 mL in 1 TUBEGEL701

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
75710-078QB SKIN LAB HAND SANITIZER (ETHYL ALCOHOL) GEL [QUORUM BIO PHARMACEUTICAL CO., LTD.]1Legacy NDC, 1 package rows20200424_a3f41864-ae14-694e-e053-2a95a90a148e.zip

Products#

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

DailyMed product names page 1 of 1 · 13 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
75710-07875710-078-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 11 matching rows.

Name, UNII, Kind table
NameUNIIKind
GALACTOSEX2RN3Q8DNEIACT
SODIUM ALGINATEC269C4G2ZQIACT
POVIDONE, UNSPECIFIEDFZ989GH94EIACT
HYALURONATE SODIUMYSE9PPT4THIACT
GLYCERINPDC6A3C0OXIACT
DIBASIC POTASSIUM PHOSPHATECI71S98N1ZIACT
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE0A5MM307FCIACT
WATER059QF0KO0RIACT
ALOE VERA LEAFZY81Z83H0XIACT
ARGININE94ZLA3W45FIACT
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
a3f4179f-5500-c6d7-e053-2995a90ab4a1a3f41864-ae14-694e-e053-2a95a90a148e2020-04-21Exact identifier
spl id: a3f4179f-5500-c6d7-e053-2995a90ab4a1
spl set id: a3f41864-ae14-694e-e053-2a95a90a148e

Reported adverse events (FAERS/openFDA)#

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