FDA.reportPublic FDA data

Uncle Buds Hand Sanitizer

Manufacturer
CBH International LLC | TAKA USA Inc. dba Cosmetic Innovations
Effective date
2021-01-10
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-01 22:57:24

Label at a glance#

ProductUncle Buds Hand Sanitizer
Active ingredientBENZALKONIUM CHLORIDE
Label structure10 sections

Dosage and administration

Wet hands thoroughly with product and allow to dry without wiping. Children under 6 years of age should be supervised when using this product. Not recommended for infants.

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium Chloride 0.1% w/w

Purpose

OTC - PURPOSE SECTION

Antiseptic

Use

INDICATIONS & USAGE SECTION

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

Warnings

WARNINGS SECTION

For external use only

When using this product

OTC - WHEN USING SECTION

  • Keep out of eyes. In case of eye contact, flush with plenty of water and seek medical advice.

Stop use and ask a doctor if

OTC - STOP USE SECTION

  • Irritation or redness develops

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. Children under 6 years of age should be supervised when using this product. Not recommended for infants.

Other Information

OTHER SAFETY INFORMATION

Store at room temperature. Avoid excessive heat.

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Aloe Vera Leaf, Caesalpinia Spinosa Gum, Canola Oil, Diethylene Glycol Monoethyl Ether, Ethylhexylglycerin, Glycerin, Phenoxyethanol, Safflower Oil, Water

Questions?

OTC - QUESTIONS SECTION

Visit Unclebudshemp.com

Bottle Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

bottle labelbottle label

Products#

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

DailyMed product names page 1 of 1 · 12 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
72680-01072680-010-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 10 matching rows.

Name, UNII, Kind table
NameUNIIKind
SAFFLOWER OIL65UEH262ISIACT
DIETHYLENE GLYCOL MONOETHYL ETHERA1A1I8X02BIACT
PHENOXYETHANOLHIE492ZZ3TIACT
ALOE VERA LEAFZY81Z83H0XIACT
CAESALPINIA SPINOSA RESINWL3883U2POIACT
ETHYLHEXYLGLYCERIN147D247K3PIACT
CANOLA OIL331KBJ17RKIACT
WATER059QF0KO0RIACT
GLYCERINPDC6A3C0OXIACT
BENZALKONIUM CHLORIDEF5UM2KM3W7ACTIB

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
efa96ddf-c563-0b14-e053-2a95a90a1b23a18dc5b6-4e10-84c9-e053-2a95a90af6d12022-12-12WarningsExact identifier
spl set id: a18dc5b6-4e10-84c9-e053-2a95a90af6d1

Reported adverse events (FAERS/openFDA)#

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