Le Vital Sweet Pea

Manufacturer
Ningbo Liyuan Daily Chemical Products Co., Ltd.
Effective date
2016-05-11
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-02 01:26:52

Label at a glance#

ProductLe Vital Sweet Pea
Active ingredientALCOHOL
Label structure8 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Mecicical Ingredient

Ethyl Alcohol 62%

Purpose

Antiseptic

OTC - PURPOSE SECTION

Features

To decrease bacteria on the skin that could cause disease.

  • Recommended for repeated use.
  • Use anywhere without water.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. In case of accidental ingestion, seek professional assistance or contact a Poison Control Center immediately.

INDICATIONS & USAGE SECTION

Le Vital ® Signature

sweet pea

hand sanitizer 

DOSAGE & ADMINISTRATION SECTION

Directions

  • Wet hands thoroughly with product and rub until dry without wiping
  • For children under 6, use only under adult supervision.
  • Not recommended for infants

WARNINGS SECTION

Warning

  • For external use only - hands
  • Flammable, keep away from heat and flame
  • Discontinue if skin becomes irritated and ask a doctor

CAUTION: For external use only. This product was not tested on animals.

When using this product

  • Keep out of eyes. In case of contact with eyes, flush thoroughly with water.
  • Do not inhale or ingest.
  • Avoid contact with broken skin.

Other information

  • Do not store above 105°F.
  • May discolor some fabrics.
  • Harmful to wood finishes and plastics.

INACTIVE INGREDIENT SECTION

Non-Medicinal

water, isopropyl alcohol, glycerin, carbomer, aminomethyl propanol, parfum, propylene glycol, isopropyl myristate, aloe barbadensis leaf juice, tacopheryl acetate

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Sweet PeaSweet Pea

Products#

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

DailyMed product names page 1 of 1 · 12 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
76176-20276176-202-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 10 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
33101c62-fa70-2c69-e054-00144ff8d46c33101c62-fa6f-2c69-e054-00144ff8d46c2016-05-11WarningsExact identifier
spl id: 33101c62-fa70-2c69-e054-00144ff8d46c
spl set id: 33101c62-fa6f-2c69-e054-00144ff8d46c

Reported adverse events (FAERS/openFDA)#

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