FDA.reportPublic FDA data

Advanced Hand SanitizerRefreshin

Manufacturer
Davion, Inc | Brands International Corp.
Effective date
2020-03-13
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:03:56

Label at a glance#

ProductAdvanced Hand SanitizerRefreshin
Active ingredientALCOHOL
Label structure9 sections

Dosage and administration

Apply small amounts to hands rub hands together vigorously until dry supervise children in the use of this product

Storage and handling

Store below 110°F (43° C) may discolor certain fabrics or surfaces

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 70%

Purpose

OTC - PURPOSE SECTION

Antiseptic

Use

INDICATIONS & USAGE SECTION

To reduce bacteria on skin

Warnings

WARNINGS SECTION

​Flammable, Keep away from fire or flame.

For external use only.

When using this product

OTC - WHEN USING SECTION

do not use in or near the eyes. In case of contact, rinse eyes thoroughly with water

Stop use and ask a doctor if

OTC - ASK DOCTOR SECTION

irritation or redness develops

Keep out of reach of children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

Directions

DOSAGE & ADMINISTRATION SECTION

  • Apply small amounts to hands
  • rub hands together vigorously until dry
  • supervise children in the use of this product

Other information

STORAGE AND HANDLING SECTION

Store below 110°F (43° C)

may discolor certain fabrics or surfaces

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Water, Isopropyl Alcohol, Glycerin, Carbomer, Aminomethyl Propano, Fragrance, Propylene Glycol, Isopropyl Myristate, Aloe Barbadensis Leaf Juice (Aloe Vera), Tocopheryl Acetate (Vitamin E).

Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

NDC 42669-070-05

Perfect Purity®

Advanced Hand Sanitizer Refreshing

Compare to Purell® Advanced Hand Sanitizer*

Kills 99.99% of Germs without Water

Leaves hands feeling soft

MOISTURE-RICH

5 oz (148 ml)

LabelLabel

NDC 42669-070-32  

Perfect Purity®

Advanced Hand Sanitizer Refreshing

Compare to Purell® Advanced Hand Sanitizer*

Kills 99.99% of Germs without Water

FRESH GEL

MOISTURIZING FORMULA

PARABEN FREE

DYE FREE

32 FL OZ (946 mL)

Label 1Label 1

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
6c13b22c-b3ba-4127-b768-0132dd5ab0d1Product name120230829

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
42669-070-052022-01-28C16284748780-1d6a99b39-bb9a-a426-e053-dadaa90af4c22ffb010d-db46-4099-a136-0e9b0e079daa
42669-070-322022-01-28C16284748780-1d6a99b39-bb9a-a426-e053-dadaa90af4c22ffb010d-db46-4099-a136-0e9b0e079daa

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
42669-070-05Advanced Hand SanitizerRefreshin148 mL in 1 BOTTLELIQUID1481
42669-070-32Advanced Hand SanitizerRefreshin946 mL in 1 BAGLIQUID9461

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
42669-070ADVANCED HAND SANITIZERREFRESHIN (ETHYL ALCOHOL 70%) LIQUID [DAVION, INC]1Legacy NDC, 2 package rows20200314_2ffb010d-db46-4099-a136-0e9b0e079daa.zip

Products#

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

DailyMed product names page 1 of 1 · 12 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
42669-07042669-070-05, 42669-070-32

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 10 matching rows.

Name, UNII, Kind table
NameUNIIKind
ALCOHOL3K9958V90MACTIB
WATER059QF0KO0RIACT
ISOPROPYL ALCOHOLND2M416302IACT
GLYCERINPDC6A3C0OXIACT
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE0A5MM307FCIACT
AMINOMETHYLPROPANOLLU49E6626QIACT
PROPYLENE GLYCOL6DC9Q167V3IACT
ISOPROPYL MYRISTATE0RE8K4LNJSIACT
ALOE VERA LEAFZY81Z83H0XIACT
.ALPHA.-TOCOPHEROL ACETATE9E8X80D2L0IACT

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
5e81c639-0e59-4535-a9c0-b292087461ca2ffb010d-db46-4099-a136-0e9b0e079daa2020-03-13WarningsExact identifier
spl id: 5e81c639-0e59-4535-a9c0-b292087461ca
spl set id: 2ffb010d-db46-4099-a136-0e9b0e079daa

Reported adverse events (FAERS/openFDA)#

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