FDA.reportPublic FDA data

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 01:20:23

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, carbomer, fragrance, triethanolamine.

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

89 mL in 1 BOTTLE NDC: 41366-017-01

89ml label89ml label

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
581662ethanol 70 % Topical GelPSN3
581662ethanol 0.7 ML/ML Topical GelSCD3
581662ethanol 70 % Topical GelSY3
581662ethyl alcohol 70 % Topical GelSY3

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
41366-017-012024-01-20C16284748780-1f386c64a-07b4-0266-e053-dadaa90a7c1aZhejiang Meimi Technology Co., Ltd. Hand Sanitizer 41366-017-01
41366-017-012023-01-30C16284748780-1f386c64a-07b4-0266-e053-dadaa90a7c1aZhejiang Meimi Technology Co., Ltd. Hand Sanitizer 41366-017-01

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
41366-017-01Hand Sanitizer89 mL in 1 BOTTLEGEL893

Products#

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

DailyMed product names page 1 of 1 · 8 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
41366-01741366-017-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 7 matching rows.

Name, UNII, Kind table
NameUNIIKind
TROLAMINE9O3K93S3TKIACT
WATER059QF0KO0RIACT
ALCOHOL3K9958V90MACTIB
PROPYLENE GLYCOL6DC9Q167V3IACT
LEMON24RS0A988OIACT
GLYCERINPDC6A3C0OXIACT
POLYACRYLIC ACID (250000 MW)9G2MAD7J6WIACT

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 SanitizerHAND SANITIZERZhejiang Meimi Technology Co., Ltd.bf399508-bd29-0d90-e053-2995a90a067f2025-12-06WarningsExact identifier
ndc (package): 41366-017-01
ndc (product): 41366-017
ndc11 (package): 41366001701
spl id: 454588b7-63fd-bf46-e063-6394a90adb4d
spl set id: bf399508-bd29-0d90-e053-2995a90a067f

Reported adverse events (FAERS/openFDA)#

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