FDA.reportPublic FDA data

CARTE BLANCHE HAND SANIZITER Gel

Manufacturer
ORACOS CO LTD. | EQMAXON Corp.
Effective date
2020-10-28
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:32:34

Label at a glance#

ProductCARTE BLANCHE HAND SANIZITER Gel
Active ingredientALCOHOL
Label structure1 sections

Label contents#

Full prescribing information#

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

CARTE BLANCHE HAND SANIZITER GELCARTE BLANCHE HAND SANIZITER GEL

OTC - ACTIVE INGREDIENT SECTION

OTC - ASK DOCTOR SECTION

OTC - DO NOT USE SECTION

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

OTC - PURPOSE SECTION

OTC - STOP USE SECTION

OTC - WHEN USING SECTION

INACTIVE INGREDIENT SECTION

INDICATIONS & USAGE SECTION

WARNINGS SECTION

DOSAGE & ADMINISTRATION 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
75201-500-012022-01-28C16284748780-1d6a99b39-9737-a426-e053-dadaa90af4c275201-500-01 CARTE BLANCHE HAND SANIZITER GEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
75201-500-01CARTE BLANCHE HAND SANIZITER Gel500 mL in 1 BOTTLE, PUMPGEL5001

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
75201-500CARTE BLANCHE HAND SANIZITER GEL (ETHYL ALCOHOL) GEL [ORACOS CO LTD.]1Legacy NDC, 1 package rows20201029_b2b4e867-3ad3-fe6c-e053-2995a90a2214.zip

Products#

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

DailyMed product names page 1 of 1 · 11 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
75201-50075201-500-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 9 matching rows.

Name, UNII, Kind table
NameUNIIKind
GLYCERINPDC6A3C0OXIACT
WATER059QF0KO0RIACT
ALOE VERA LEAFZY81Z83H0XIACT
PROPYLENE GLYCOL6DC9Q167V3IACT
ALCOHOL3K9958V90MACTIB
HYALURONATE SODIUMYSE9PPT4THIACT
BUTYLENE GLYCOL3XUS85K0RAIACT
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE0A5MM307FCIACT
AMINOMETHYLPROPANOLLU49E6626QIACT

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
b2b4e867-3ad4-fe6c-e053-2995a90a2214b2b4e867-3ad3-fe6c-e053-2995a90a22142020-10-28Exact identifier
spl id: b2b4e867-3ad4-fe6c-e053-2995a90a2214
spl set id: b2b4e867-3ad3-fe6c-e053-2995a90a2214

Reported adverse events (FAERS/openFDA)#

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