85472-010

Manufacturer
Zhejiang Gaorong Cosmetic Co., Ltd. | Zhejiang TR Technology Co., Ltd.
Effective date
2026-05-20
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 01:59:08

Label at a glance#

ProductHand Sanitizer
Active ingredientALCOHOL
Label structure9 sections

Indications and uses

· To decrease bacteria on the skin that could cause disease. · When water, soap and towel are not available. · Recommended for repeated use.

Dosage and administration

· Spray product in your palm and rub hands together until dry. · For children under 6, use only under adult supervision. · Not recommended for infants.

Storage and handling

· Do not store above 105°F. · May discolor some fabrics. · Harmful to wood finishes and plastics.

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

ETHYL ALCOHOL 70%

Purpose

OTC - PURPOSE SECTION

ANTISEPTIC

Uses

INDICATIONS & USAGE SECTION

· To decrease bacteria on the skin that could cause disease.
· When water, soap and towel are not available.
· Recommended for repeated use.

Warnings

WARNINGS SECTION

For external use only. Flammable. Keep away from fire or flame.

When using this product:

OTC - WHEN USING SECTION

·Keep out of eyes, ears, or mouth.
·In case of eye contact, flush eyes thoroughly with water.
·Avoid contact with broken skin.
·Do not inhale or ingest.

Stop use and ask a doctor if

OTC - WHEN USING SECTION

· Redness or irritation develop.
· Condition persists for more than 72 hours.

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

· Children should be supervised by an adult when using this product.
· If swallowed, get medical help or contact a Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

· Spray product in your palm and rub hands together until dry.
· For children under 6, use only under adult supervision.
· Not recommended for infants.

Other Information

STORAGE AND HANDLING SECTION

· Do not store above 105°F.
· May discolor some fabrics.
· Harmful to wood finishes and plastics.

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Water, Glycerin, Dipropylene Glycol, Glycereth-26, Fragrance, Butylene Glycol, Leuconostoc/ Radish Root Ferment Filtrate, Aloe Barbadensis Leaf Juice, Phenoxyethanol.
May Contain: Red 40 Lake (CI 16035), Red 33 Lake (CI 17200), Red 4 Lake (CI 14700), Yellow 5 Lake (CI 19140:1), Blue 1 Lake (CI 42090:2).

85472-010-01

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

0101

85472-010-02

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

0202

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1041849ethanol 70 % Topical SprayPSN1
1041849ethanol 0.7 ML/ML Topical SpraySCD1
1041849ethanol 70 % Topical SpraySY1

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
85472-010-01Hand Sanitizer35 mL in 1 BOTTLELIQUID351
85472-010-02Hand Sanitizer40 mL in 1 BOTTLELIQUID401

Products#

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

DailyMed product names page 1 of 1 · 17 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
85472-01085472-010-01, 85472-010-02

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 15 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 SanitizerETHYL ALCOHOLZhejiang Gaorong Cosmetic Co., Ltd.523cd61a-c2ee-2c70-e063-6294a90a6c772026-05-20WarningsExact identifier
ndc (package): 85472-010-01
ndc (package): 85472-010-02
ndc (product): 85472-010
ndc11 (package): 85472001002
ndc11 (package): 85472001001
spl id: 523cd61a-c2ef-2c70-e063-6294a90a6c77
spl set id: 523cd61a-c2ee-2c70-e063-6294a90a6c77

Reported adverse events (FAERS/openFDA)#

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