FDA.reportPublic FDA data

Alcohol Free 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 23:27:27

Label at a glance#

ProductAlcohol Free Hand Sanitizer
Active ingredientBENZALKONIUM CHLORIDE, POLYAMINOPROPYL BIGUANIDE
Label structure8 sections

Indications and uses

For personal hand sanitizing and reduce bacteria on the skin,Recommended for repeated use.

Dosage and administration

Apply liberally to the hands and gently rub to dry.

Label contents#

Full prescribing information#

Active Ingredient(s)

OTC - ACTIVE INGREDIENT SECTION

Polyaminopropyl Biguanide 0.28%,Benzalkonium Chloride 0.13%

Purpose

OTC - PURPOSE SECTION

Antiseptic

USES

INDICATIONS & USAGE SECTION

For personal hand sanitizing and reduce bacteria on the skin,Recommended for repeated use.

Warnings

WARNINGS SECTION

For external use only

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. Stop use and ask a doctor if irritation and redness develop. Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away

Directions

DOSAGE & ADMINISTRATION SECTION

Apply liberally to the hands and gently rub to dry.

Inactive ingredients

INACTIVE INGREDIENT SECTION

Aqua(Water), Glycerin, Hydroxypropyl Methylcellulose, Sodium Benzoate, PEG/Ppg-17/6 Copolymer, Parfum, Disodium EDTA

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

500500303025025010001000500050006060300300100100

Products#

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

DailyMed product names page 1 of 1 · 11 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
75438-00575438-005-01, 75438-005-02, 75438-005-03, 75438-005-04, 75438-005-05, 75438-005-06, 75438-005-07, 75438-005-08

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 9 matching rows.

Name, UNII, Kind table
NameUNIIKind
BENZALKONIUM CHLORIDEF5UM2KM3W7ACTIB
GLYCERINPDC6A3C0OXIACT
HYPROMELLOSE, UNSPECIFIED3NXW29V3WOIACT
WATER059QF0KO0RIACT
POLYAMINOPROPYL BIGUANIDEDT9D8Z79ETACTIB
BENZYL ALCOHOLLKG8494WBHIACT
SODIUM BENZOATEOJ245FE5EUIACT
PPG-17OV0Q322E0UIACT
EDETATE DISODIUM ANHYDROUS8NLQ36F6MMIACT

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-ba7b-44e2-e053-2995a90a3312a414fa9f-0e87-3239-e053-2a95a90a10412021-01-21WarningsExact identifier
spl set id: a414fa9f-0e87-3239-e053-2a95a90a1041

Reported adverse events (FAERS/openFDA)#

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