FDA.reportPublic FDA data

Hand Sanitizing Spring Rain

Manufacturer
Base4 Ventures, LLC.
Effective date
2021-11-30
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
legacy-cache
Hydrated at
2026-08-01 22:25:28

Label at a glance#

ProductHand Sanitizing Spring Rain
Active ingredientALCOHOL
Label structure6 sections

Dosage and administration

Adults and children 2 years and older: Remove wipe from package and wipe hands to disinfect. Allow skin to dry.  Children under 2 years; Consult a doctor before use.

Label contents#

Full prescribing information#

Active Ingredients

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 75%

Purpose

OTC - PURPOSE SECTION

Antimicrobial

Use

INDICATIONS & USAGE SECTION

decreases bacteria on skin

Warnings

WARNINGS SECTION

  • For external use only
  • Flammable
  • Keep away from heat and flame.

Do not use 

OTC - DO NOT USE SECTION

if your are allergic to any of the ingredients

When using this product

OTC - WHEN USING SECTION

do not get into eyes. If contact occurs, rinse thoroughly with water.

Stop use and ask a doctor

OTC - STOP USE SECTION

if irritation or rash develops and continues for more than 72 hours.

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

Directions

DOSAGE & ADMINISTRATION SECTION

  • Adults and children 2 years and older: Remove wipe from package and wipe hands to disinfect. Allow skin to dry. 
  • Children under 2 years; Consult a doctor before use.

Inactive ingredients:

INACTIVE INGREDIENT SECTION

Aloe Barbadensis Leaf Extract, Aminomethyl Propanol, Carbomer, Glycerin, Propylene Glycol, Water

Package Labeling:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Label5Label5

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
62651-07562651-075-50

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 7 matching rows.

Name, UNII, Kind table
NameUNIIKind
ALOE VERA LEAFZY81Z83H0XIACT
AMINOMETHYLPROPANOLLU49E6626QIACT
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE0A5MM307FCIACT
GLYCERINPDC6A3C0OXIACT
PROPYLENE GLYCOL6DC9Q167V3IACT
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
086ca455-e145-e3a1-e063-6294a90a3638a9df7ab4-5e2c-6e36-e053-2a95a90a19ae2023-10-23WarningsExact identifier
spl set id: a9df7ab4-5e2c-6e36-e053-2a95a90a19ae

Reported adverse events (FAERS/openFDA)#

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