HAND SANITIZER LIQUID SPRAY

Manufacturer
Weckerle Cosmetics LLC
Effective date
2020-07-13
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:21:29

Label at a glance#

ProductHAND SANITIZER liquid
Active ingredientAlcohol
Label structure9 sections

Dosage and administration

Put enough product in your palm to cover hands and rub hands together briskly until dry. Children under 6 years of age should be supervised when using the product.

Storage and handling

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

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

Drug Facts

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 70% v/v

Purpose

OTC - PURPOSE SECTION

Anti-microbial

Use

INDICATIONS & USAGE SECTION

  • Hand Sanitizer to help reduce bacteria on skin

Warnings

WARNINGS SECTION

Flammable. Keep away from fire or flame.

For external use only

OTC - WHEN USING SECTION

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

OTC - STOP USE SECTION

Stop use and ask a doctor if irritation or rash appears and lasts.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. If swallowed, get medical help or contact Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

  • Put enough product in your palm to cover hands and rub hands together briskly until dry.
  • Children under 6 years of age should be supervised when using the 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 , Glycerin, Propanediol, Panthenol, Fragrance, Aloe Barbadensis Leaf Juice, Green 5.

PRINCIPAL DISPLAY PANEL - 100 mL Bottle Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

precos

HAND
SANITIZER
LIQUID SPRAY

KILLS
99.9%
OF GERMS
& BACTERIA

WITH ALOE VERA
& PRO VITAMIN B5
TO MOISTURIZE

OCEAN

3.4 FL OZ / 100mL

PRINCIPAL DISPLAY PANEL - 100 mL Bottle Label
PRINCIPAL DISPLAY PANEL - 100 mL Bottle Label

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1041849ethanol 70 % Topical SprayPSN1
1041849ethanol 0.7 ML/ML Topical SpraySCD1
1041849ethanol 70 % Topical SpraySY1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
62516-002-012022-01-28C16284748780-1d6a99b39-abdd-a426-e053-dadaa90af4c2HAND SANITIZER LIQUID SPRAY

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
62516-002-01HAND SANITIZER liquid100 mL in 1 BOTTLEAEROSOL, SPRAY1001

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
62516-002HAND SANITIZER LIQUID (ALCOHOL) AEROSOL, SPRAY [WECKERLE COSMETICS LLC]1Legacy NDC, 1 package rows20200716_341ddbba-1560-4477-a6d9-2b7dee5fdc57.zip

Products#

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

DailyMed product names page 1 of 1 · 8 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
62516-00262516-002-01

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
107449f3-e427-475c-b256-7089f2d58f8b341ddbba-1560-4477-a6d9-2b7dee5fdc572020-07-13WarningsExact identifier
spl id: 107449f3-e427-475c-b256-7089f2d58f8b
spl set id: 341ddbba-1560-4477-a6d9-2b7dee5fdc57

Reported adverse events (FAERS/openFDA)#

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