FDA.reportPublic FDA data

Hand Sanitizer Sling with Essential Oil Fresh Rosewater

Manufacturer
Base4 Ventures, LLC.
Effective date
2021-11-30
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-01 22:25:32

Label at a glance#

ProductHand Sanitizer Sling with Essential Oil Fresh Rosewater
Active ingredientALCOHOL
Label structure7 sections

Indications and uses

Hand sanitizer to help decrease bacteria on the skin that could cause disease. Recommended for repeated use

Dosage and administration

Place enough product in your palm to thoroughly cover your hands Rub hands together briskly until dry Children 6 years of age should be supervised when using this product

Label contents#

Full prescribing information#

Active ingredients

OTC - ACTIVE INGREDIENT SECTION

Alcohol Dentat. 66% v/v

Purpose

OTC - PURPOSE SECTION

Antimicrobial

Uses

INDICATIONS & USAGE SECTION

  • Hand sanitizer to help decrease bacteria on the skin that could cause disease.
  • Recommended for repeated use

Warnings

WARNINGS SECTION

  • Flammable. Keep away from heat and 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 

OTC - STOP USE SECTION

if irritation or rash appears and lasts.

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

  • Place enough product in your palm to thoroughly cover your hands
  • Rub hands together briskly until dry
  • Children 6 years of age should be supervised when using this product

Other information

SPL UNCLASSIFIED SECTION

Do not store above 110°F (43°C)

  • May discolor some fabrics or surfaces

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water, Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Fragrance, Aminomethyl Propanol, Rosa Canina Fruit Oil, May Contain: D&C Red No. 33, FD&C Red No. 4.

Package Labeling:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

BottleBottle

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
62651-06862651-068-01

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
CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED)59TL3WG5COIACT
AMINOMETHYLPROPANOLLU49E6626QIACT
ROSA CANINA FRUIT OILCR7307M3QZIACT
ALCOHOL3K9958V90MACTIB
WATER059QF0KO0RIACT

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
086c76d7-ec20-6051-e063-6294a90a3695c71714d1-fb59-5dc1-e053-2a95a90a4b492023-10-23WarningsExact identifier
spl set id: c71714d1-fb59-5dc1-e053-2a95a90a4b49

Reported adverse events (FAERS/openFDA)#

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