SeneGence Hand Sanitizer

Manufacturer
SGII, Inc
Effective date
2020-07-07
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 23:21:50

Label at a glance#

ProductSeneGence Hand Sanitizer
Active ingredientALCOHOL
Label structure11 sections

Storage and handling

Other information Store between 15-30°C (59-86°F). Avoid freezing and excessive heat above 40°C (104°F)..

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active Ingredient

Alcohol 62% v/v

OTC - PURPOSE SECTION

Purpose

Antiseptic

WARNINGS SECTION

  • For external use only.
  • Flammable, Keep away from heat or flame.

OTC - WHEN USING SECTION

When using this product keep out of eyes, ears and mouth. If case of contact with eyes, rinse eyes thoroughly with water.

OTC - STOP USE SECTION

Stop use and ask a doctor if irritation or rash occurs. These may be signs of serious condition.

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.

INDICATIONS & USAGE SECTION

Uses

  • Hand Sanitizer to help reduce bacteria that potentialy can cause disease.
  • For use when soap and water are not available.

DOSAGE & ADMINISTRATION SECTION

Directions

  • Place enough product on hands to cover all surfaces.
  • Rub hands together until dry
  • Supervise children under 6 years of age when using this product to avoid swallowing

STORAGE AND HANDLING SECTION

Other information

  • Store between 15-30°C (59-86°F).
  • Avoid freezing and excessive heat above 40°C (104°F)..

INACTIVE INGREDIENT SECTION

Inactive ingredients Aloe Barbadensis Leaf Juice, Carthamus Tinctorius (Safflower) Oleosomes, Cymbopogon Flexuosus (Lemongrass) Oil, Fragrance (Parfum), Glycerin, Helianthus Annuus (Sunflower) Seed Oil, Hydroxyethylcellulose, Lonicera Caprifolium (Honeysuckle) Flower Extract, Lonicera Japonica (Honeysuckle) Flower Extract, PEG-40 Hydrogenated Castor Oil, Rosmarinus Officinalis (Rosemary) Leaf Extract, Sodium Hyaluronate, Water (Aqua), Yellow 10 (CI 47005). May contain Isopropyl Alcohol.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

SGHS2SGHS2

Products#

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NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
72644-62872644-628-02

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 15 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
d2affc41-2805-95ff-e053-2995a90a648fa9e3b8c4-fe89-2869-e053-2a95a90a56542021-12-08WarningsExact identifier
spl set id: a9e3b8c4-fe89-2869-e053-2a95a90a5654

Reported adverse events (FAERS/openFDA)#

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