FDA.reportPublic FDA data

Hand Sanitizer

Manufacturer
Chico's FAS, Inc.
Effective date
2020-12-07
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:34:40

Label at a glance#

ProductHand Sanitizer
Active ingredientALCOHOL
Label structure12 sections

Dosage and administration

Put enough product in your palms to cover hands. Rub hands together until dry. Children under 6 years of age should be supervised when using this product.

Storage and handling

Store in closed container in a dry location between 15-30°C (59-86°F) Avoid freezing and excessive heat above 40°C (104°F) May discolor some fabrics Harmful to wood finishes and plastics Dispose in accordance with all applicable federal, state and local regulations

Label contents#

Full prescribing information#

Active Ingredient(s)

OTC - ACTIVE INGREDIENT SECTION

Alcohol 70% v/v. Purpose: Antiseptic

Purpose

OTC - PURPOSE SECTION

Antiseptic, Hand Sanitizer

Use

INDICATIONS & USAGE SECTION

Hand sanitizing to reduce bacteria on skin. No rinsing required. For use when soap and water are not available.

Warnings

WARNINGS SECTION

For external use only. Flammable. Keep away from heat or flame

Do not use

OTC - DO NOT USE SECTION

  • in children less than 2 months of age
  • on open skin wounds

OTC - WHEN USING SECTION

When using this product. Not for internal use, do not swallow or inhale. If swallowed, do not induce vomiting. Consult a physician or a Poison Control Center immediately. Keep out of eyes. In case of thoroughly with cold water. Avoid contact with broken skin.

OTC - STOP USE SECTION

Stop use and ask a doctor if irritation or rash persists for more than 24 hours. These may be signs of a serious condition.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children and pets. Children must be supervised when using this product.

Directions

DOSAGE & ADMINISTRATION SECTION

  • Put enough product in your palms to cover hands. Rub hands together until dry.
  • Children under 6 years of age should be supervised when using this product.

Other information

STORAGE AND HANDLING SECTION

  • Store in closed container in a dry location between 15-30°C (59-86°F)
  • Avoid freezing and excessive heat above 40°C (104°F)
  • May discolor some fabrics
  • Harmful to wood finishes and plastics
  • Dispose in accordance with all applicable federal, state and local regulations

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water (Aqua), Acrylates/C10-30 alkyl acrylate crosspolymer, Aloe barbadensis leaf extract, Fragrance, Triethanolamine

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Front labelFront labellabellabel50 mL NDC: 65657-070-01

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
581662ethanol 70 % Topical GelPSN1
581662ethanol 0.7 ML/ML Topical GelSCD1
581662ethanol 70 % Topical GelSY1
581662ethyl alcohol 70 % Topical GelSY1

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
BarcodeEAN-130194301031914GTIN-13: 0194301031914
EAN-13: 0194301031914
GTIN-12: 194301031914
UPC-A: 194301031914
GTIN storage (14 digits): 00194301031914		Label 1.jpg

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
65657-070-012022-01-28C16284748780-1d6a99b39-4b95-a426-e053-dadaa90af4c2b4cdac55-12f7-4e72-e053-2995a90aab2b

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
65657-070-01Hand Sanitizer50 mL in 1 BOTTLE, PLASTICGEL501

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
65657-070HAND SANITIZER (ALCOHOL) GEL [CHICO'S FAS, INC.]1Legacy NDC, 1 package rows20201207_b4cdac55-12f7-4e72-e053-2995a90aab2b.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
65657-07065657-070-01

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
ALOE VERA LEAFZY81Z83H0XIACT
CARBOMER INTERPOLYMER TYPE A (55000 CPS)59TL3WG5COIACT
TROLAMINE9O3K93S3TKIACT
WATER059QF0KO0RIACT
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
b4cdac55-12f6-4e72-e053-2995a90aab2bb4cdac55-12f7-4e72-e053-2995a90aab2b2020-12-07WarningsExact identifier
spl id: b4cdac55-12f6-4e72-e053-2995a90aab2b
spl set id: b4cdac55-12f7-4e72-e053-2995a90aab2b

Reported adverse events (FAERS/openFDA)#

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