WhiskCare 375

Manufacturer
Whisk Products, Inc.
Effective date
2023-06-26
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-01 21:29:33

Label at a glance#

ProductWhiskCare 375 Fragrance Free
Active ingredientALCOHOL
Label structure7 sections

Dosage and administration

Place 5 grams or palmful of product in one hand. Spread on hands and rub into skin until dry. Place a smaller amount (2.5 grams) into one hand and spread over both hands and wrists. Rub into skin until dry. Children should be supervised while using this product.

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 70% v/v

Purpose

OTC - PURPOSE SECTION

Skin Sanitizer

Use

INDICATIONS & USAGE SECTION

Hand sanitizer to help reduce amount of bacteria on the skin

Warnings

WARNINGS SECTION

Flammable. Keep away from fire or flame.

For external use only. If swallowed, seek medical attention.

When using this product do not use around or near the eyes. If contact occurs, flush eyes with water and contact a doctor immediately.

Stop use and consult a doctor when skin irritation appears and lasts.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children.

Directions

DOSAGE & ADMINISTRATION SECTION

  • Place 5 grams or palmful of product in one hand.
  • Spread on hands and rub into skin until dry.
  • Place a smaller amount (2.5 grams) into one hand and spread over both hands and wrists.
  • Rub into skin until dry.
  • Children should be supervised while using this product.

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Water, Glycerin, Carbomer, Propylene Glycol, Diisopropylamine

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Drum LabelDrum Label

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
65585-37965585-379-01

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
ff089a1b-b4c6-53e1-e053-6394a90a8875febb4eef-c1c0-5bc4-e053-6394a90a7c5c2023-06-26WarningsExact identifier
spl id: ff089a1b-b4c6-53e1-e053-6394a90a8875
spl set id: febb4eef-c1c0-5bc4-e053-6394a90a7c5c

Reported adverse events (FAERS/openFDA)#

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