Hand Sanitizer

Manufacturer
Zhejiang Meimi Technology Co., Ltd.
Effective date
2024-01-20
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-06-01 00:07:40

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, blue 1.

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

59 mL in 1 BOTTLE NDC: 41366-051-01

59ml label59ml label

59 mL in 1 BOTTLE NDC: 41366-051-02

59ml label59ml label

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
581662ethanol 70 % Topical GelPSN2
581662ethanol 0.7 ML/ML Topical GelSCD2
581662ethanol 70 % Topical GelSY2
581662ethyl alcohol 70 % Topical GelSY2

FDA-Initiated Inactive NDC Indexing#

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
41366-051-01Hand Sanitizer59 mL in 1 BOTTLEGEL592
41366-051-02Hand Sanitizer59 mL in 1 BOTTLEGEL592

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
41366-051HAND SANITIZER GEL [ZHEJIANG MEIMI TECHNOLOGY CO., LTD.]2Legacy NDC, 2 package rows20240121_dcebf021-9d6b-bfae-e053-2a95a90a0510.zip

Products#

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

DailyMed product names page 1 of 1 · 11 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
41366-05141366-051-01, 41366-051-02

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 10 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
0f5d2f46-98b3-e276-e063-6394a90a6c02dcebf021-9d6b-bfae-e053-2a95a90a05102024-01-20WarningsExact identifier
spl id: 0f5d2f46-98b3-e276-e063-6394a90a6c02
spl set id: dcebf021-9d6b-bfae-e053-2a95a90a0510

Reported adverse events (FAERS/openFDA)#

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