FDA.reportPublic FDA data

Instant Hand Sanitizer

Manufacturer
Fujian Jinghua Biotechnology Co.,Ltd.
Effective date
2020-06-08
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-01 23:27:28

Label at a glance#

ProductInstant Hand Sanitizer
Active ingredientALCOHOL
Label structure9 sections

Indications and uses

To decrease bacteria on the skin that could cause disease Recommended for repearted use

Dosage and administration

Wet hands thoroughly with product and allow to dry without wiping. For children under 6, use only under adult supervision. No recommended forinfants

Storage and handling

Store below 106"F(41 C) May dicolor certain fabrics or surfaces

Label contents#

Full prescribing information#

Active Ingredient(s)

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 75.0%

Purpose

OTC - PURPOSE SECTION

Antiseptic

USES

INDICATIONS & USAGE SECTION

  • To decrease bacteria on the skin that could cause disease
  • Recommended for repearted use

WARNINGS

WARNINGS SECTION

  • Flammable, keep away from fire or flame
  • For external use only-hands

When Using This Product

OTC - WHEN USING SECTION

When Using This Product do not use in or near the eyes. In case of contact, rinse eyes thoroughly with water .Do not inhale or ingest. Avoid contact with broken skin. Stop use and ask a doctor if skin irritation develops. Keep out of reach of children. In case of accidental ingestion,see professional assistance or contact a Poison Control Center immediately

Directions

DOSAGE & ADMINISTRATION SECTION

Wet hands thoroughly with product and allow to dry without wiping. For children under 6, use only under adult supervision. No recommended forinfants

OTHER INFORMATION

STORAGE AND HANDLING SECTION

  • Store below 106"F(41 C)
  • May dicolor certain fabrics or surfaces

INACTIVE INGREDIENTS

INACTIVE INGREDIENT SECTION

Aqua(Water),Glycerin, Carbomer, Sodium Hydroxide, Parfum, Ethylhexyl Glycerin, Aloe Barbadensis Leaf Extract

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

10010050050030ml30ml25025010001000500050006060300300

Products#

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

DailyMed product names page 1 of 1 · 9 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
75438-00775438-007-01, 75438-007-02, 75438-007-03, 75438-007-04, 75438-007-05, 75438-007-06, 75438-007-07, 75438-007-08

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 8 matching rows.

Name, UNII, Kind table
NameUNIIKind
GLYCERINPDC6A3C0OXIACT
CARBOMER 934Z135WT9208IACT
WATER059QF0KO0RIACT
ALCOHOL3K9958V90MACTIB
ALOE VERA LEAFZY81Z83H0XIACT
SODIUM HYDROXIDE55X04QC32IIACT
ETHYLHEXYLGLYCERIN147D247K3PIACT
BENZYL ALCOHOLLKG8494WBHIACT

Source Document#

Source XML · Source PDF

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
b9649a1a-b8cb-4b8f-e053-2995a90a3d24a418f456-8810-2359-e053-2995a90a28ea2021-01-21WarningsExact identifier
spl set id: a418f456-8810-2359-e053-2995a90a28ea

Reported adverse events (FAERS/openFDA)#

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