FDA.reportPublic FDA data

FB HYDRATING HAND SANITIZER

Manufacturer
NINGBO MEITELI COSMETICS CO., LTD
Effective date
2024-05-13
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 21:02:28

Label at a glance#

ProductFB HYDRATING HAND SANITIZER
Active ingredientDEHYDRATED ALCOHOL
Label structure12 sections

Dosage and administration

Spray enough sanitizer in your palm to cover both hands. Rub hands together briskly until dry. Children under six should be supervised.

Storage and handling

Protect the product in this container from excessive heat and direct sun. Store below 104 0F (40 0C). May discolor certain fabrics.

Label contents#

Full prescribing information#

Active Ingredient(s)

OTC - ACTIVE INGREDIENT SECTION

ETHYL ALCOHOL：70%

Purpose

OTC - PURPOSE SECTION

Antiseptic

Use

INDICATIONS & USAGE SECTION

hand sanitizer to help reduce bacteria on the skin.

Warnings

WARNINGS SECTION

Flammable: Keep away from fire or flame.
For external use only.

Do not use

OTC - DO NOT USE SECTION

Children under two years old, please do not use

OTC - WHEN USING SECTION

When using this product keep out of eyes, ears and mouth.
In case of contact, rinse eyes thoroughly with water.
Avoid contact with broken skin.

OTC - STOP USE SECTION

Stop use and see a doctor if irritation or rash appears and lasts.

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

Spray enough sanitizer in your palm to cover both hands. Rub hands
together briskly until dry. Children under six should be supervised.

Other information

STORAGE AND HANDLING SECTION

Protect the product in this container from excessive heat and direct sun.
Store below 104 0F (40 0C).
May discolor certain fabrics.

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water, Glycerin, Fragrance, Red 40 Lake (CI 16035), Red 33 (CI 17200)

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

labellabel

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
75541-011FB HYDRATING HAND SANITIZER GEL [NINGBO MEITELI COSMETICS CO., LTD]1Unmatched20240517_185374d5-8ddc-c8d3-e063-6294a90a8254.zip

Products#

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

DailyMed product names page 1 of 1 · 6 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
75541-01175541-011-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 5 matching rows.

Name, UNII, Kind table
NameUNIIKind
D&C RED NO. 339DBA0SBB0LIACT
FD&C RED NO. 40WZB9127XOAIACT
WATER059QF0KO0RIACT
GLYCERINPDC6A3C0OXIACT
DEHYDRATED ALCOHOL3K9958V90MACTIB

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
45a40570-29df-7eb0-e063-6294a90ac16c185374d5-8ddc-c8d3-e063-6294a90a82542025-12-10WarningsExact identifier
spl set id: 185374d5-8ddc-c8d3-e063-6294a90a8254

Reported adverse events (FAERS/openFDA)#

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