HAND SANITIZER

Manufacturer
Shangrao Baolijie Daily Necessities Co,Ltd
Effective date
2024-07-17
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 20:58:41

Label at a glance#

ProductHAND SANITIZER
Active ingredientALCOHOL
Label structure12 sections

Dosage and administration

Directions:①wet hands thoroughly with product and rub into skin until dry. ②children under 6 years of age should be supervised by an adult when using.

Storage and handling

No data available

Label contents#

Full prescribing information#

Active Ingredient(s)

OTC - ACTIVE INGREDIENT SECTION

Alcohol 75%

Purpose

OTC - PURPOSE SECTION

Antimicrobial

Use

INDICATIONS & USAGE SECTION

USE:hand sanitizer to help reduce bacteria on the skin that may cause disease.

Warnings

WARNINGS SECTION

Warnings: ①for extemal use only. ②Flammable. Keep away from heat and fame.

Do not use

OTC - DO NOT USE SECTION

Donnotuse on da maged skin(cuts, abrasionseczema, sunburn)f you areallergic to any of the ingredients in this product.

OTC - WHEN USING SECTION

When using this product:avoid contact with face, eyes, and broken skin. In case of eye contact, flush with plenty of water
and seek medical advice.

OTC - STOP USE SECTION

Stop use and ask a doctor if:iritation or redness develops.

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.

Directions

DOSAGE & ADMINISTRATION SECTION

Directions:①wet hands thoroughly with product and rub into skin until dry.

②children under 6 years of age should be supervised by an adult when using.

Other information

STORAGE AND HANDLING SECTION

No data available

Inactive ingredients

INACTIVE INGREDIENT SECTION

water, glycerol, aloe vera extract, carbomer

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

1122

Products#

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

DailyMed product names page 1 of 1 · 6 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
84559-00184559-001-01, 84559-001-02

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 5 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
2e17033c-895d-3e6a-e063-6294a90a6c051d6d1f26-cb45-d531-e063-6294a90ad4d52025-02-14WarningsExact identifier
spl set id: 1d6d1f26-cb45-d531-e063-6294a90ad4d5

Reported adverse events (FAERS/openFDA)#

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