Core Home Canyon Biotch Clear Sanitizer Gel Alc70

Manufacturer
Core Home
Effective date
2022-07-12
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
legacy-cache
Hydrated at
2026-08-01 21:56:56

Label at a glance#

ProductHand Sanitizer
Active ingredientALCOHOL
Label structure12 sections

Indications and uses

■ For hand washing to decrease bacteria on the skin. ■ Recommended for repeat use

Dosage and administration

■ Rub a 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.

Storage and handling

■ Store below 105ºF ■ May discolor fabrics

Label contents#

Full prescribing information#

Active Ingredients

OTC - ACTIVE INGREDIENT SECTION

Alcohol 70%

Purpose

OTC - PURPOSE SECTION

Antiseptic

Uses

INDICATIONS & USAGE SECTION

■ For hand washing to decrease bacteria on the skin. ■ Recommended for repeat use

Warnings

WARNINGS SECTION

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

Does not contain grain alcohol, do not drink. If taken internally will produce serious gastric disturbances

When using this product

OTC - WHEN USING SECTION

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

Stop use and ask a doctor

OTC - STOP USE SECTION

■ Redness or irritation develops

■ Conditions worsens

■ If condition persists 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 a 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

STORAGE AND HANDLING SECTION

■ Store below 105ºF

■ May discolor fabrics

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Water, Glycerin, Fragrance, Carbomer, Aloe Extract, Sodium Hydroxide

Questions?

OTC - QUESTIONS SECTION

■ 1-844-884-4910

Package Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

package labelpackage label

FDA-Initiated Inactive NDC Indexing#

Products#

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

DailyMed product names page 1 of 1 · 7 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
80424-00280424-002-08, 80424-002-16, 80424-002-33

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
e3a34951-3847-b46e-e053-2995a90a34fbae7fceed-74c3-df3d-e053-2a95a90a781b2022-07-12WarningsExact identifier
spl id: e3a34951-3847-b46e-e053-2995a90a34fb
spl set id: ae7fceed-74c3-df3d-e053-2a95a90a781b

Reported adverse events (FAERS/openFDA)#

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