FDA.reportPublic FDA data

b+free Hand Sanitizer Spray with Aloe Vera and Vitamin E

Manufacturer
b+free
Effective date
2022-09-13
Label type
HUMAN OTC DRUG LABEL
Version
4
Source
legacy-cache
Hydrated at
2026-08-01 21:53:50

Label at a glance#

Productb free Hand Sanitizer with Aloe Vera and Vitamin E
Active ingredientALCOHOL
Label structure9 sections

Indications and uses

hand sanitizer to decrease bacteria on the skin. recommended for repeated use for use when soap and water are not available.

Dosage and administration

wet hands thoroughly with product and allow to dry without wiping supervise children under 6 years of age when using this product to avoid swallowing

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Ethyl alcohol 70%

Purpose

OTC - PURPOSE SECTION

Antiseptic

Uses

INDICATIONS & USAGE SECTION

  • hand sanitizer to decrease bacteria on the skin.
  • recommended for repeated use
  • for use when soap and water are not available.

Warnings

WARNINGS SECTION

Flammable, keep away from fire/flame. For external use only

Do not use

OTC - DO NOT USE SECTION

  • in children less than 2 months of age
  • on open skin wounds.

When using this product

OTC - WHEN USING SECTION

  • do not get into eyes. In case of contact, rinse eyes thoroughly with water
  • do not inhale or ingest.

Stop and ask doctor if

OTC - STOP USE SECTION

  • irritation and redness develop
  • condition persists 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

  • wet hands thoroughly with product and allow to dry without wiping
  • supervise children under 6 years of age when using this product to avoid swallowing

Other information

SPL UNCLASSIFIED SECTION

  • store between 15-30ºC (59-86ºF)
  • avoid freezing and excessive heat above 40ºC (104ºF)
  • may discolor certain fabrics or surfaces

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water, Glycerin, Fragrance, Tocopheryl Acetate (VITAMIN E), Aloe Barbadensis Leaf Extract

Package Labeling:20 mL

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Label6Label6

Package Labeling:50 mL

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Label7Label7

Package Labeling:100 mL

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Label8Label8

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
90120-00290120-002-01, 90120-002-02, 90120-002-03

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
WATER059QF0KO0RIACT
GLYCERINPDC6A3C0OXIACT
.ALPHA.-TOCOPHEROL ACETATE9E8X80D2L0IACT
ALOE VERA LEAFZY81Z83H0XIACT
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
e894a3c5-2e66-729d-e053-2995a90a7c87ae6bd776-8d84-1a13-e053-2a95a90a3e2e2022-09-13WarningsExact identifier
spl id: e894a3c5-2e66-729d-e053-2995a90a7c87
spl set id: ae6bd776-8d84-1a13-e053-2a95a90a3e2e

Reported adverse events (FAERS/openFDA)#

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