Hand Rx Hand Sanitizer

Manufacturer: Ningbo Liyuan Daily Chemical Products Co., Ltd.
Effective date: 2020-05-18
Label type: HUMAN OTC DRUG LABEL
Version: 1
Source: legacy-cache
Hydrated at: 2026-08-01 23:30:21

Label at a glance#

ProductHand Rx Hand Sanitizer

Active ingredientALCOHOL

Label structure10 sections

Dosage and administration

wet hands thoroughly with product and allow to dry without wiping. for children under 6, use only under adult supervision not recommended for infants

Label contents#

Full prescribing information#

Active Ingredient(s)

OTC - ACTIVE INGREDIENT SECTION

Alcohol 62% v/v. Purpose: Antiseptic

Purpose

OTC - PURPOSE SECTION

Antiseptic

Use

INDICATIONS & USAGE SECTION

to decrease bacteria on the skin
recommended for repeated use

Warnings

WARNINGS SECTION

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

Do not use

OTC - DO NOT USE SECTION

not recommended for infants
avoid contact with broken skin
do not inhale or ingest

OTC - WHEN USING SECTION

When using this product keep out of eyes. In case of contact with eyes, flush eyes thoroughly with water.

Stop use and ask a doctor if irritation or rash occurs.

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

wet hands thoroughly with product and allow to dry without wiping.
for children under 6, use only under adult supervision
not recommended for infants

Inactive ingredients

INACTIVE INGREDIENT SECTION

water, glycerin, propylene glycol, carbomer

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Hand Rx Hand Sanitizer

Antiseptic Solution

8 FL OZ. (236 ml)

419148F

Products#

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

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

Hand Rx Hand Sanitizer
ALCOHOL
GLYCERIN
PROPYLENE GLYCOL
WATER
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
76176-330	76176-330-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 5 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
GLYCERIN	PDC6A3C0OX	IACT
PROPYLENE GLYCOL	6DC9Q167V3	IACT
WATER	059QF0KO0R	IACT
ALCOHOL	3K9958V90M	ACTIB
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE	0A5MM307FC	IACT

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
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
a5f06b3d-e84c-9520-e053-2a95a90ab0d0			a5f18177-1370-0aa7-e053-2995a90a62fa	2020-05-18	Warnings	Exact identifier spl id: a5f06b3d-e84c-9520-e053-2a95a90ab0d0 spl set id: a5f18177-1370-0aa7-e053-2995a90a62fa

Reported adverse events (FAERS/openFDA)#

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