ProNature EARTH CONSCIOUS HAND SANITIZER with Aloe Vera Extract

Manufacturer
JIANGSU HANHE DAILY CHEMICALS CO., LTD.
Effective date
2021-11-02
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
full-release
Hydrated at
2026-05-31 23:44:45

Label at a glance#

ProductProNature EARTH CONSCIOUS HAND SANITIZER with Aloe Vera Extract
Active ingredientALCOHOL
Label structure10 sections

Dosage and administration

Place enough product in palm to thoroughly cover hands Briskly rub hands together until dry Children under 6 years of age should be supervised when using this product

Storage and handling

Store below 104F (40C)

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 69% v/v

Purpose

OTC - PURPOSE SECTION

Antibacterial Agent

Use

INDICATIONS & USAGE SECTION

For hand washing to decrease bacteria on the skin

Recommended for repeated use

Warnings

WARNINGS SECTION

For external use only.

Non Medical. Flammable. Keep away from fire or flame

When using this product, do not use in or near eyes, In case of contact, rinse eyes thoroughly with water

OTC - STOP USE SECTION

Discontinue use and contact a doctor if irritation and redness develop and condition persists for more than 72 hours

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. If swallowed, get medical help or contact a poison control center right away

Directions

DOSAGE & ADMINISTRATION SECTION

  • Place enough product in palm to thoroughly cover hands
  • Briskly rub hands together until dry
  • Children under 6 years of age should be supervised when using this product

Other Information

STORAGE AND HANDLING SECTION

Store below 104F (40C)

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water, Carbomer, Triethanolamine, Glycerin, PEG-40 Hydrogenated Caster Oil, Aloe Barbadensis (Aloe Vera) Leaf Extract, Parfum

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image descriptionimage description

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
2287763ethanol 69 % Topical GelPSN3
2287763ethanol 0.69 ML/ML Topical GelSCD3
2287763ethanol 69 % Topical GelSY3

FDA-Initiated Inactive NDC Indexing#

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
73027-207-01ProNature EARTH CONSCIOUS HAND SANITIZER with Aloe Vera Extract60 mL in 1 BOTTLEGEL603
73027-207-02ProNature EARTH CONSCIOUS HAND SANITIZER with Aloe Vera Extract300 mL in 1 BOTTLEGEL3003
73027-207-03ProNature EARTH CONSCIOUS HAND SANITIZER with Aloe Vera Extract500 mL in 1 BOTTLEGEL5003
73027-207-04ProNature EARTH CONSCIOUS HAND SANITIZER with Aloe Vera Extract30 mL in 1 BOTTLEGEL303

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
73027-207PRONATURE EARTH CONSCIOUS HAND SANITIZER WITH ALOE VERA EXTRACT (ALCOHOL) GEL [JIANGSU HANHE DAILY CHEMICALS CO., LTD.]3Legacy NDC, 4 package rows20211104_de020f1f-4141-4665-9704-ccb1729bfc32.zip

Products#

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

DailyMed product names page 1 of 1 · 7 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
73027-20773027-207-01, 73027-207-02, 73027-207-03, 73027-207-04

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 6 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
cfda6a1e-8fd1-595b-e053-2995a90a5069de020f1f-4141-4665-9704-ccb1729bfc322021-11-02WarningsExact identifier
spl id: cfda6a1e-8fd1-595b-e053-2995a90a5069
spl set id: de020f1f-4141-4665-9704-ccb1729bfc32

Reported adverse events (FAERS/openFDA)#

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