Hand Sanitizer

Manufacturer
Ningbo Meiteli Cosmetic Co., Ltd.
Effective date
2020-05-14
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:13:09

Label at a glance#

ProductHand Sanitizer
Active ingredientALCOHOL
Label structure11 sections

Dosage and administration

Put enough sanitizer in your palm to cover both hands,Rub hands together brishly until dry,Children under six should be supervised

Storage and handling

Store below 110F(43C) May discolor some fabrics or surfaces

Label contents#

Full prescribing information#

Active Ingredient(s)

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 75%

Purpose

OTC - PURPOSE SECTION

Antimicrobial

Use

INDICATIONS & USAGE SECTION

Hand Sanitizer to help reduce bacteria on the skin.

Warning

WARNINGS SECTION

Flammable. Keep away from heat or flame

For external use only.

Do not use near eyes

OTC - DO NOT USE SECTION

In case of contact rinse eyes thoroughly with water.

Stop use

OTC - STOP USE SECTION

Stop use and see a doctor if imtation or rash appears and lasts

Keep out of reach of children

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

Put enough sanitizer in your palm to cover both hands,Rub hands together brishly until dry,Children under six should be supervised

Other

STORAGE AND HANDLING SECTION

  • Store below 110F(43C)
  • May discolor some fabrics or surfaces

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water(Aqua). Glycerin, Acrylatewc10-30 Alkyl CrateCrosspolymer, Aloe Barbadensis Loaf Extract, Triethanolamine

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

112233

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1305100ethanol 75 % Topical GelPSN1
1305100ethanol 0.75 ML/ML Topical GelSCD1
1305100ethanol 75 % Topical GelSY1

FDA-Initiated Inactive NDC Indexing#

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
75541-006-01Hand Sanitizer60 mL in 1 BOTTLEGEL601
75541-006-02Hand Sanitizer119 mL in 1 BOTTLEGEL1191
75541-006-03Hand Sanitizer178 mL in 1 BOTTLEGEL1781
75541-006-04Hand Sanitizer237 mL in 1 BOTTLEGEL2371
75541-006-05Hand Sanitizer296 mL in 1 BOTTLEGEL2961
75541-006-06Hand Sanitizer476 mL in 1 BOTTLEGEL4761
75541-006-07Hand Sanitizer948 mL in 1 BOTTLEGEL9481

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
75541-006HAND SANITIZER GEL [NINGBO MEITELI COSMETIC CO., LTD.]1Legacy NDC, 7 package rows20200515_a59a50ec-9c73-5c4b-e053-2995a90aeb3f.zip

Products#

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

DailyMed product names page 1 of 1 · 7 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
75541-00675541-006-02, 75541-006-01, 75541-006-04, 75541-006-03, 75541-006-05, 75541-006-07, 75541-006-06

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 6 matching rows.

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
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
a59a50ec-9c72-5c4b-e053-2995a90aeb3fa59a50ec-9c73-5c4b-e053-2995a90aeb3f2020-05-14WarningsExact identifier
spl id: a59a50ec-9c72-5c4b-e053-2995a90aeb3f
spl set id: a59a50ec-9c73-5c4b-e053-2995a90aeb3f

Reported adverse events (FAERS/openFDA)#

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