M Skin Care Gel Hand Sanitizer 120

Manufacturer
Mingshi Technology Co., LTD
Effective date
2021-12-02
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-01 22:25:00

Label at a glance#

ProductM Skin Care Gel Hand Sanitizer 120
Active ingredientALCOHOL
Label structure9 sections

Indications and uses

To help reduce bacteria on the skin.

Dosage and administration

Apply enough product on hands to cover all surfaces. Rub hands together until dry.

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Alcohol 70%

­­­­­­­­­­­­­­­­­­­­­ Purpose

OTC - PURPOSE SECTION

Antiseptic

Uses

INDICATIONS & USAGE SECTION

To help reduce bacteria on the skin.

Warnings

WARNINGS SECTION

FLAMMABLE. Keep away from heat or flame

For External Use only. When using this product

Keep out of eyes, ears, and mouth. In case of contact with eyes, rinse eyes thoroughly with water.

Do not use with children less than 2 months of age- On open skin wounds -around eyes -in ears and mouth.

Stop use and ask a doctor if irritation or rash occurs. These may be signs of a serious condition

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, get medical help or contact a Poison Control Center immediately

Directions

DOSAGE & ADMINISTRATION SECTION

Apply enough product on hands to cover all surfaces. Rub hands together until dry.

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Water, Aloe Barbadensis, Acrylates/C10-30 Alkylacrylate crosspolymer, Triethanolamine, Tocopheryl acetate, Glycerin, Fragrance

Other Information

OTHER SAFETY INFORMATION

Store between 59-86F (15-30C). -Avoid freezing and excessive above 104 F (40C)

M Skin Care Gel Hand Sanitizer Anti-Bacterial 120ml

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

120120

FDA-Initiated Inactive NDC Indexing#

Products#

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

DailyMed product names page 1 of 1 · 9 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
73992-10273992-102-04, 73992-102-02

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

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
eff457ac-29b4-6035-e053-2a95a90a5a63a227d079-1d40-4a70-e053-2995a90a94c62022-12-16WarningsExact identifier
spl set id: a227d079-1d40-4a70-e053-2995a90a94c6

Reported adverse events (FAERS/openFDA)#

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