Hand Sanitizer

Manufacturer: Zhejiang Meimi Technology Co., Ltd.
Effective date: 2025-12-06
Label type: HUMAN OTC DRUG LABEL
Version: 3
Source: full-release
Hydrated at: 2026-06-01 01:20:27

Label at a glance#

ProductHand Sanitizer

Active ingredientALCOHOL

Label structure11 sections

Dosage and administration

Put a dime sized drop onto hands and rub together briskly until dry.

Storage and handling

Store below 110℉(43℃).

Label contents#

Full prescribing information#

Active Ingredient(s)

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 70% v/v

Purpose

OTC - PURPOSE SECTION

Antimicrobial

Use

INDICATIONS & USAGE SECTION

Uses hand sanitizer to help reduce bacteria on skin.

Warnings

WARNINGS SECTION

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

Do not use

OTC - DO NOT USE SECTION

Do not use in or near the eyes. In case of contact, rinse eyes thoroughly with water.

OTC - STOP USE SECTION

Stop use and ask a doctor if irritation, excessive redness or rash develops.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. Supervise children under 6 years of age when using this product to avoid swallowing. If swallowed, get medical help or contact a Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

Put a dime sized drop onto hands and rub together briskly until dry.

Other information

STORAGE AND HANDLING SECTION

Store below 110℉(43℃).

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water, glycerin, propylene glycol, fragrance, carbomer, triethanolamine, yellow 6, red 4.

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

59 mL in 1 BOTTLE NDC: 41366-050-01

59ml label

59 mL in 1 BOTTLE NDC: 41366-050-02

59ml label

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	SPL version
581662	ethanol 70 % Topical Gel	PSN	3
581662	ethanol 0.7 ML/ML Topical Gel	SCD	3
581662	ethanol 70 % Topical Gel	SY	3
581662	ethyl alcohol 70 % Topical Gel	SY	3

Product Linked Resources#

Resource, Code type, Value table
Resource	Code type	Value	Equivalent identifiers	Source image
Barcode	EAN-13	0049696878852	GTIN-13: 0049696878852 EAN-13: 0049696878852 GTIN-12: 049696878852 UPC-A: 049696878852 GTIN storage (14 digits): 00049696878852	59ml_1_1.jpg
Barcode	EAN-13	0049696878869	GTIN-13: 0049696878869 EAN-13: 0049696878869 GTIN-12: 049696878869 UPC-A: 049696878869 GTIN storage (14 digits): 00049696878869	59ml_1_2.jpg

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
41366-050-01	Hand Sanitizer	59 mL in 1 BOTTLE	GEL	59		3
41366-050-02	Hand Sanitizer	59 mL in 1 BOTTLE	GEL	59		3

Products#

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

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

Hand Sanitizer
ALCOHOL
GLYCERIN
CARBOMER 940
PUMPKIN
FD&C YELLOW NO. 6
FD&C RED NO. 4
PROPYLENE GLYCOL
TROLAMINE
WATER

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
41366-050	41366-050-01, 41366-050-02

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 9 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
ALCOHOL	3K9958V90M	ACTIB
GLYCERIN	PDC6A3C0OX	IACT
CARBOMER 940	4Q93RCW27E	IACT
PUMPKIN	SYW0QUB89Y	IACT
FD&C YELLOW NO. 6	H77VEI93A8	IACT
FD&C RED NO. 4	X3W0AM1JLX	IACT
PROPYLENE GLYCOL	6DC9Q167V3	IACT
TROLAMINE	9O3K93S3TK	IACT
WATER	059QF0KO0R	IACT

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
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Hand Sanitizer	HAND SANITIZER	Zhejiang Meimi Technology Co., Ltd.	dceb9358-663c-3c70-e053-2995a90a3524	2025-12-06	Warnings	Exact identifier ndc (package): 41366-050-01 ndc (package): 41366-050-02 ndc (product): 41366-050 ndc11 (package): 41366005001 ndc11 (package): 41366005002 spl id: 4545efcb-ceb9-48b0-e063-6294a90a3d9d spl set id: dceb9358-663c-3c70-e053-2995a90a3524

Reported adverse events (FAERS/openFDA)#

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