FDA.reportPublic FDA data

Hand Sanitizer Toasted Vanilla

Manufacturer
Base4 Ventures, LLC
Effective date
2019-06-13
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-02 00:07:46

Label at a glance#

ProductHand Sanitizer Toasted Vanilla
Active ingredientALCOHOL
Label structure8 sections

Dosage and administration

Rub dime sized amount between hands until dry Supervise children in the use of this product In the case of eye contact rinse eyes thoroughly with water

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Alcohol Denat. 66%

Purpose

OTC - PURPOSE SECTION

Antiseptic

Use

INDICATIONS & USAGE SECTION

  • For handwashing to decrease bacteria on the skin

Warnings

WARNINGS SECTION

For external use only.

  • Flammable. Keep away from fire & flame
  • Does not contain grain alcohol; do not drink. If taken internally will produce severe gastric disturbances

When using this product

OTC - WHEN USING SECTION

  • Avoid the eyes and mucous membranes 
  • In the case of eyes or mucous membrane contact, rinse area thoroughly with water

Stop use and ask a doctor if 

OTC - STOP USE SECTION

  • Condition worsens
  • Redness or irritation develops
  • Condition persist for more than 3 days

Keep out of reach of children. 

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, contact a doctor or Poison Control Center immediately.

Directions

DOSAGE & ADMINISTRATION SECTION

  • Rub dime sized amount between hands until dry
  • Supervise children in the use of this product
  • In the case of eye contact rinse eyes thoroughly with water

Other information

SPL UNCLASSIFIED SECTION

  • Store below 105°F
  • May discolor fabrics

Inactive ingredients:

INACTIVE INGREDIENT SECTION

Water (Aqua), Acrylates, C10-30 Alkyl Acrylate Crosspolymer, Aminomethyl Propanol, Fragrance.

Questions?

OTC - QUESTIONS SECTION

Call 1-888-988-2427

Package Labeling:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Label12Label12

Products#

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

DailyMed product names page 1 of 1 · 3 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
62651-01262651-012-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 2 matching rows.

Name, UNII, Kind table
NameUNIIKind
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
c13590c9-130e-733a-e053-2a95a90a77d7c4e5ab20-cd2f-42ad-bbfe-bf0dbedf6dd02021-04-30WarningsExact identifier
spl set id: c4e5ab20-cd2f-42ad-bbfe-bf0dbedf6dd0

Reported adverse events (FAERS/openFDA)#

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