Hand Sanitizer

Manufacturer
Shenzhen spring cosmetics co.,LTD
Effective date
2020-06-12
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-01 23:26:12

Label at a glance#

ProductHand Sanitizer
Active ingredientALCOHOL
Label structure12 sections

Dosage and administration

pump as needed into your palms and thoroughly spread on both hands

Storage and handling

Do not store above 110° F

Label contents#

Full prescribing information#

Active Ingredient(s)

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 75%

Purpose

OTC - PURPOSE SECTION

Antiseptic

Usage

INDICATIONS & USAGE SECTION

  • helps decrease bacteria on skin
  • Recommended for repeated use

Warnings

WARNINGS SECTION

For external use only.

Flammable, Keep away from fire or flame

Do not apply

OTC - DO NOT USE SECTION

around eyes

When using this product.

OTC - WHEN USING SECTION

avoid contact with eyes, In case of contact flush eves with water

Stop use and ask a doctor

OTC - STOP USE SECTION

 If irritation or redness develops condition persists for more than 72 hours

keep out of reach of Children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Children must be supervised in use of this product

Directions

DOSAGE & ADMINISTRATION SECTION

pump as needed into your palms and thoroughly spread on both hands

Other information

STORAGE AND HANDLING SECTION

Do not store above 110° F

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water, Glycerin, Propylene Glycol, Carbomer, Vitamin E

Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

NDC 76717-005-01, 76717-005-02

2 oz2 oz

8 oz8 oz

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
76717-00576717-005-01, 76717-005-02

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

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
b8c4fe2e-dd81-0ef8-e053-2995a90afc21a419da35-760b-9d36-e053-2995a90aba4f2021-01-13WarningsExact identifier
spl set id: a419da35-760b-9d36-e053-2995a90aba4f

Reported adverse events (FAERS/openFDA)#

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