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 ingredientALCOHOL
Label structure9 sections

Dosage and administration

Wet plams thoroughly with product and rub hands together until dry. Children under 6 years of age should be supervised when using this product. Not reommended for infants.

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 70%

Purpose

OTC - PURPOSE SECTION

Antiseptic

Use

INDICATIONS & USAGE SECTION

To decrease bacteria on the skin that could cause disease

Warnings

WARNINGS SECTION

For external use only.

Flammable. Keep away from heat or flame.

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.
  • Avoid contact with broken skin.
  • Do not inhale or ingest.

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 plams thoroughly with product and rub hands together until dry. Children under 6 years of age should be supervised when using this product. Not reommended for infants.

Other Information

OTHER SAFETY INFORMATION

Store at room temperature. Avoid excessive heat. May discolor some fabrics.

Inactive Ingredients

INACTIVE INGREDIENT SECTION

C12-15 Alkyl Benzoate, Carbomer, Glycerin, Sodium Hydroxide, 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 · 8 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
72680-00772680-007-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 6 matching rows.

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
efa9574d-48d2-3905-e053-2995a90aace2a09d3d1d-8b18-12b7-e053-2995a90a10ee2022-12-12WarningsExact identifier
spl set id: a09d3d1d-8b18-12b7-e053-2995a90a10ee

Reported adverse events (FAERS/openFDA)#

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