AP HanSan

Manufacturer
WhiskProducts, Inc. | Whisk Products, Inc.
Effective date
2023-12-07
Label type
HUMAN OTC DRUG LABEL
Version
5
Source
full-release
Hydrated at
2026-06-01 00:03:41

Label at a glance#

ProductAP HanSan
Active ingredientALCOHOL
Label structure7 sections

Dosage and administration

Place a small amount of spray into the hands. Spread on hands and rub into skin until dry. Place a smaller amount in one hand and spread over both hands and wrists. Rub into skin until dry. Children should be supervised while using this product.

Label contents#

Full prescribing information#

​Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 60% v/v

Purpose

OTC - PURPOSE SECTION

Skin Sanitizer

​Use

INDICATIONS & USAGE SECTION

To help reduce the amount of bacteria on the skin

​Warnings

WARNINGS SECTION

Flammable.  Keep away from fire or flame.

For external use only.  If swallowed seek medical attention.

When using this product do not use around or near the eyes.  If contact occurs, flus eyes iwth water and contact doctor immediately.

Stop use and consult a doctor when skin irritation appears and lasts.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children.

​Directions

DOSAGE & ADMINISTRATION SECTION

  • Place a small amount of spray into the hands.
  • Spread on hands and rub into skin until dry.
  • Place a smaller amount in one hand and spread over both hands and wrists.
  • Rub into skin until dry.
  • Children should be supervised while using this product.

​Inactive Ingredients

INACTIVE INGREDIENT SECTION

Water, Glycerin, Propylene Glycol

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

1 Gallon ShortNeck Bottle Label1 Gallon ShortNeck Bottle Label

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1367692ethanol 60 % Topical SprayPSN5
1367692ethanol 0.6 ML/ML Topical SpraySCD5
1367692ethanol 60 % Topical SpraySY5

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
65585-580-01AP HanSan3.785 L in 1 BOTTLESPRAY3.7855

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
65585-580AP HANSAN (ALCOHOL) SPRAY [WHISKPRODUCTS, INC.]5Current NDC, Legacy NDC, 1 package rows20231208_e212fd90-f4e4-44c4-bfb7-16e313c30be9.zip

Products#

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

DailyMed product names page 1 of 1 · 5 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
65585-58065585-580-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 4 matching rows.

Name, UNII, Kind table
NameUNIIKind
WATER059QF0KO0RIACT
GLYCERINPDC6A3C0OXIACT
PROPYLENE GLYCOL6DC9Q167V3IACT
ALCOHOL3K9958V90MACTIB

Source Document#

Source XML · Source PDF

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
AP HanSanALCOHOLWhiskProducts, Inc.e212fd90-f4e4-44c4-bfb7-16e313c30be92023-12-07WarningsExact identifier
ndc (package): 65585-580-01
ndc (product): 65585-580
ndc11 (package): 65585058001
spl id: 0bf2073f-50d0-529d-e063-6294a90abfd4
spl set id: e212fd90-f4e4-44c4-bfb7-16e313c30be9

Reported adverse events (FAERS/openFDA)#

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