Advanced Hand Sanitizer

Manufacturer
Ningbo Meiteli Cosmetic Co., Ltd.
Effective date
2020-04-30
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-05-31 23:08:49

Label at a glance#

ProductAdvanced Hand 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 70%

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

Alcohol Denat,Water(aqua),Glycerin,Carbomer,Aminomethylpropanol,Aloe Barbadensis Leaf Juice,Tocopherol

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

44113322

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
582753ethanol 70 % Topical SolutionPSN2
582753ethanol 0.7 ML/ML Topical SolutionSCD2
582753ethanol 70 % Topical SolutionSY2
582753ethyl alcohol 70 % Topical SolutionSY2

FDA-Initiated Inactive NDC Indexing#

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
75541-005-01Advanced Hand Sanitizer30 mL in 1 BOTTLELIQUID302
75541-005-02Advanced Hand Sanitizer236 mL in 1 BOTTLELIQUID2362
75541-005-03Advanced Hand Sanitizer1000 mL in 1 BOTTLELIQUID10002
75541-005-04Advanced Hand Sanitizer50 mL in 1 BOTTLELIQUID502
75541-005-05Advanced Hand Sanitizer59 mL in 1 BOTTLELIQUID592
75541-005-06Advanced Hand Sanitizer100 mL in 1 BOTTLELIQUID1002
75541-005-07Advanced Hand Sanitizer250 mL in 1 BOTTLELIQUID2502
75541-005-08Advanced Hand Sanitizer480 mL in 1 BOTTLELIQUID4802
75541-005-09Advanced Hand Sanitizer3780 mL in 1 BOTTLELIQUID37802
75541-005-10Advanced Hand Sanitizer500 mL in 1 BOTTLELIQUID5002

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
75541-005ADVANCED HAND SANITIZER LIQUID [NINGBO MEITELI COSMETIC CO., LTD.]2Legacy NDC, 10 package rows20200430_a3dc6d53-0bf8-7aa7-e053-2995a90a2595.zip

Products#

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

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

NDC Codes#

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 7 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
a47b3627-124a-e8b1-e053-2995a90ab93ca3dc6d53-0bf8-7aa7-e053-2995a90a25952020-04-30WarningsExact identifier
spl id: a47b3627-124a-e8b1-e053-2995a90ab93c
spl set id: a3dc6d53-0bf8-7aa7-e053-2995a90a2595

Reported adverse events (FAERS/openFDA)#

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