FDA.reportPublic FDA data

BotaneCo Hand Sanitizer

Manufacturer
Botaneco Inc | EC Labs | Natures Formulae Health Products Ltd.
Effective date
2020-08-19
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
legacy-cache
Hydrated at
2026-08-01 23:16:37

Label at a glance#

ProductBotaneCo Hand Sanitizer
Active ingredientALCOHOL
Label structure10 sections

Indications and uses

Hand sanitizer to help reduce bacteria on the skin. Recommended for repeated use.

Dosage and administration

Rub thoroughly into hands for at least 30 seconds. Allow to dry. Supervise children when they use this product. For repeated use and personal domestic use.

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 70% v/v

Purpose

OTC - PURPOSE SECTION

Antiseptic

Uses

INDICATIONS & USAGE SECTION

Hand sanitizer to help reduce bacteria on the skin. Recommended for repeated use.

Warnings

WARNINGS SECTION

Flammable. Keep away from fire or flame.

For External Use Only.

OTC - WHEN USING SECTION

When using this product avoid contact with eyes. In case of eye contact immediately flush eyes with water, call a doctor. Avoid contact with broken skin.

OTC - STOP USE SECTION

Discontinue use if irriation or redness deelops. If condition persists for more than 72 hours, consult a dcotor.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. Children should only use this product under adult supervision.

Directions

DOSAGE & ADMINISTRATION SECTION

Rub thoroughly into hands for at least 30 seconds. Allow to dry. Supervise children when they use this product. For repeated use and personal domestic use.

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Water, Carthamus tinctorius (safflower) oleosomes, glycerin, hydroxyethyl cellulose or polyacrylate crosspolymer-6, fragrance

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

PDPPDP

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
74661-00174661-001-01

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
WATER059QF0KO0RIACT
GLYCERINPDC6A3C0OXIACT
AMMONIUM ACRYLOYLDIMETHYLTAURATE, DIMETHYLACRYLAMIDE, LAURYL METHACRYLATE AND LAURETH-4 METHACRYLATE COPOLYMER, TRIMETHYLOLPROPANE TRIACRYLATE CROSSLINKED (45000 MPA.S)Q7UI015FF9IACT
FRAGRANCE LAVENDER & CHIA F-153480SXS9CO2TZKIACT
CARTHAMUS TINCTORIUS (SAFFLOWER) OLEOSOMES9S60Q72309IACT
ALCOHOL3K9958V90MACTIB
HYDROXYETHYL CELLULOSE, UNSPECIFIEDT4V6TWG28DIACT

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
0b77422b-2877-87e6-e063-6294a90a970eaaa840e9-f5af-69fb-e053-2995a90ad58c2023-12-01WarningsExact identifier
spl set id: aaa840e9-f5af-69fb-e053-2995a90ad58c

Reported adverse events (FAERS/openFDA)#

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