Hand sanitizer

Manufacturer
Guangzhou Baihua Co., Ltd
Effective date
2025-12-14
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-06-01 01:23:34

Label at a glance#

ProductHand sanitizer
Active ingredientALCOHOL
Label structure14 sections

Dosage and administration

Spray enough product in your palm to thoroughly cover your hands, rub hands together briskly until dry, recommended to repeated use, children under 6 years of age should be supervised when using this product

Storage and handling

Protect the product in this container from excessive heat and direct sun. Store below 104 °F(40 °C) May discolorcertain fabrics

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 70%

Purpose

OTC - PURPOSE SECTION

Antiseptic

Use

INDICATIONS & USAGE SECTION

Hand sanitizer to decrease bacteria on the skin, Recommended for repeated use.

Warnings

WARNINGS SECTION

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

Do not use

OTC - DO NOT USE SECTION

if irritation and rash occurs. These may be signs of serious condition.

When Using

OTC - WHEN USING SECTION

When using this product keep out of eye, ears, and mouth. In case of contact with eyes, rinse eyes thoroughly with water. Avoid contact with broken skin

Stop Use

OTC - STOP USE SECTION

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

Ask Doctor

OTC - ASK DOCTOR SECTION

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

Keep Out Of Reach Of Children

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

Directions

DOSAGE & ADMINISTRATION SECTION

Spray enough product in your palm to thoroughly cover your hands, rub hands together briskly until dry, recommended to repeated use, children under 6 years of age should be supervised when using this product

Other information

STORAGE AND HANDLING SECTION

Protect the product in this container from excessive heat and direct sun.
Store below 104 °F(40 °C)
May discolorcertain fabrics

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water, Fragrance, Aloe Barbadensis Leaf Water,Glycerin, Tocopheryl Acetate, Yellow 6 (Cl 15985), Red 33(C1 17200)

Questions

OTC - QUESTIONS SECTION

Call 718-975-2586

PRINCIPAL DISPLAY PANEL

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

11

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1041849ethanol 70 % Topical SprayPSN2
1041849ethanol 0.7 ML/ML Topical SpraySCD2
1041849ethanol 70 % Topical SpraySY2

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
BarcodeEAN-130198926008238GTIN-13: 0198926008238
EAN-13: 0198926008238
GTIN-12: 198926008238
UPC-A: 198926008238
GTIN storage (14 digits): 00198926008238
Label.jpg

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
77665-105-01Hand sanitizer30 mL in 1 BOTTLESPRAY302

Products#

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

DailyMed product names page 1 of 1 · 10 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
77665-10577665-105-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 8 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
Hand sanitizerHAND SANITIZER SPRAYGuangzhou Baihua Co., Ltd3aab2ced-cc6f-2c20-e063-6294a90a36d92025-12-14WarningsExact identifier
ndc (package): 77665-105-01
ndc (product): 77665-105
ndc11 (package): 77665010501
spl id: 45f542d1-3afb-3f2c-e063-6294a90a2d62
spl set id: 3aab2ced-cc6f-2c20-e063-6294a90a36d9

Reported adverse events (FAERS/openFDA)#

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