FDA.reportPublic FDA data

Zhejiang Meimi Technology Co., Ltd. HAND SANITIZER GEL 59ml 41366-073-01

Manufacturer
Zhejiang Meimi Technology Co., Ltd.
Effective date
2022-10-16
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 21:51:30

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 fire 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(Parfum), carbomer, triethanolamine, T-Butyl Alcohol, Denatonium Benzoate, Red 33, Blue 1.

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

59 mL in 1 BOTTLE

NDC: 41366-073-01

59ml label59ml label

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
41366-07341366-073-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 10 matching rows.

Name, UNII, Kind table
NameUNIIKind
TERT-BUTYL ALCOHOLMD83SFE959IACT
TROLAMINE9O3K93S3TKIACT
WATER059QF0KO0RIACT
PROPYLENE GLYCOL6DC9Q167V3IACT
GLYCERINPDC6A3C0OXIACT
CARBOMER 9404Q93RCW27EIACT
ALCOHOL3K9958V90MACTIB
DENATONIUM BENZOATE ANHYDROUSM5BA6GAF1OIACT
D&C RED NO. 339DBA0SBB0LIACT
FD&C BLUE NO. 1H3R47K3TBDIACT

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
eb225f45-90b6-eb3e-e053-2a95a90aaca4eb225f45-90b7-eb3e-e053-2a95a90aaca42022-10-16WarningsExact identifier
spl id: eb225f45-90b6-eb3e-e053-2a95a90aaca4
spl set id: eb225f45-90b7-eb3e-e053-2a95a90aaca4

Reported adverse events (FAERS/openFDA)#

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