87660-102

Manufacturer
Guangdong Yanze Biotechnology Co., Ltd.
Effective date
2026-05-17
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 01:57:50

Label at a glance#

ProductHand Sanitizer
Active ingredientALCOHOL
Label structure8 sections

Indications and uses

Hand sanitizer to help reduce bacteria that potentially can cause disease. For use when soap and water are not available.

Dosage and administration

Apply into hand and thoroughly spray on both hands, rub until dry. Supervise children under 6 years of age when using this product to avoid swallowing.

Storage and handling

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

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Alcohol 62% v/v

Purpose

OTC - PURPOSE SECTION

Antiseptic

Uses

INDICATIONS & USAGE SECTION

Hand sanitizer to help reduce bacteria that potentially can cause disease. For use when soap and water are not available.

Warning

WARNINGS SECTION

Flammable.

Keep away from fire and flames.

For external use only.

Do not use

OTC - DO NOT USE SECTION

it near eye area. In case of contact, rinse eye thoroughly with water.

Stop use and ask a doctor

OTC - STOP USE SECTION

if irritation or rash appears and lasts.

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, get medical help or contact a Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

Apply into hand and thoroughly spray on both hands, rub until dry. Supervise children under 6 years of age when using this product to avoid swallowing.

Other information

STORAGE AND HANDLING SECTION

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

Inactive ingredients

INACTIVE INGREDIENT SECTION

Glycerin, Water, Fragrance

87660-102-01

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

REDRED

PINKPINK

YELLOWYELLOW

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1020364ethanol 62 % Topical SprayPSN1
1020364ethanol 0.62 ML/ML Topical SpraySCD1
1020364ethanol 62 % Topical SpraySY1
1020364ethyl alcohol 62 % Topical SpraySY1

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
BarcodeEAN-130810200259463GTIN-13: 0810200259463
EAN-13: 0810200259463
GTIN-12: 810200259463
UPC-A: 810200259463
GTIN storage (14 digits): 00810200259463
hong.jpg
BarcodeEAN-130810200259470GTIN-13: 0810200259470
EAN-13: 0810200259470
GTIN-12: 810200259470
UPC-A: 810200259470
GTIN storage (14 digits): 00810200259470
fen.jpg
BarcodeEAN-130810200259487GTIN-13: 0810200259487
EAN-13: 0810200259487
GTIN-12: 810200259487
UPC-A: 810200259487
GTIN storage (14 digits): 00810200259487
huang.jpg

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
87660-102-01Hand Sanitizer10 mL in 1 BOTTLESPRAY101

Products#

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

DailyMed product names page 1 of 1 · 5 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
87660-10287660-102-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 4 matching rows.

Name, UNII, Kind table
NameUNIIKind
ALCOHOL3K9958V90MACTIB
GLYCERINPDC6A3C0OXIACT
FRAGRANCE 135765EM498GW35IACT
WATER059QF0KO0RIACT

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 SanitizerALCOHOLGuangdong Yanze Biotechnology Co., Ltd.520e7b2b-e24e-5ce7-e063-6294a90a986d2026-05-17WarningsExact identifier
ndc (package): 87660-102-01
ndc (product): 87660-102
ndc11 (package): 87660010201
spl id: 520e7b2b-e24f-5ce7-e063-6294a90a986d
spl set id: 520e7b2b-e24e-5ce7-e063-6294a90a986d

Reported adverse events (FAERS/openFDA)#

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