Orchard De Flore Instant Hand Sanitizer

Manufacturer
SONORA CORPORATION
Effective date
2020-06-11
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-05-31 23:17:16

Label at a glance#

ProductOrchard De Flore Instant Hand Sanitizer
Active ingredientALCOHOL
Label structure7 sections

Indications and uses

• For hand sanitizing to decrease bacteria on the skin • Recommended for repeated use

Dosage and administration

Squeeze appropriate amount of sanitizer on to hands and rub together until dry. Use as needed. For children under 6, use with adult supervision. Not recommended for infants.

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 75%

Purpose

OTC - PURPOSE SECTION

Antiseptic

Uses

INDICATIONS & USAGE SECTION

• For hand sanitizing to decrease bacteria on the skin

• Recommended for repeated use

Warnings

WARNINGS SECTION

For external use only

When using this product:

OTC - WHEN USING SECTION

avoid contact with eyes. In case of eye contact, flush eyes with water.

Stop use and ask a doctor if:

OTC - STOP USE SECTION

irritation or redness develops, or if condition persists for more than 72 hours.

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed get medical help or contact a Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

Squeeze appropriate amount of sanitizer on to hands and rub together until dry. Use as needed. For children under 6, use with adult supervision. Not recommended for infants.

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Water, Aloe Barbadensis Leaf Extract, Acrylates/C10-30 alkyl Acrylate Crosspolymer, Tetrahydroxypropyl Ethylenediamine.

Package Labeling:250ml

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Label2Label2

Package Labeling:500ml

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Label3Label3

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1305100ethanol 75 % Topical GelPSN2
1305100ethanol 0.75 ML/ML Topical GelSCD2
1305100ethanol 75 % Topical GelSY2

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
78733-015-002023-01-30C16284748780-1f386c64a-4475-0266-e053-dadaa90a7c1aOrchard De Flore Instant Hand Sanitizer
78733-015-012023-01-30C16284748780-1f386c64a-4475-0266-e053-dadaa90a7c1aOrchard De Flore Instant Hand Sanitizer

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
78733-015-00Orchard De Flore Instant Hand Sanitizer250 mL in 1 BOTTLEGEL2502
78733-015-01Orchard De Flore Instant Hand Sanitizer500 mL in 1 BOTTLEGEL5002

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
78733-015ORCHARD DE FLORE INSTANT HAND SANITIZER (ALCOHOL) GEL [SONORA CORPORATION]2Legacy NDC, 2 package rows20200612_53424496-afd8-4cbd-bd60-3274b6de5ef7.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
78733-01578733-015-00, 78733-015-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 5 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
a7d22e04-ce43-27c0-e053-2995a90a2b2053424496-afd8-4cbd-bd60-3274b6de5ef72020-06-11WarningsExact identifier
spl id: a7d22e04-ce43-27c0-e053-2995a90a2b20
spl set id: 53424496-afd8-4cbd-bd60-3274b6de5ef7

Reported adverse events (FAERS/openFDA)#

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