WhiskCare 375

Manufacturer
Whisk Products, Inc.
Effective date
2024-07-26
Label type
HUMAN OTC DRUG LABEL
Version
4
Source
full-release
Hydrated at
2026-06-01 00:16:07

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 60% 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 doctor immediately.

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, Propylene Glycol, Carbomer, Glycerin, Triethanolamine

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Product Label - 55 Gallon DrumProduct Label - 55 Gallon Drum

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
581658ethanol 60 % Topical GelPSN4
581658ethanol 0.6 ML/ML Topical GelSCD4
581658ethanol 60 % Topical GelSY4

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
65585-378-01WhiskCare 375Fragrance Free0.8 L in 1 BAGGEL0.84
65585-378-01WhiskCare 375Fragrance Free12 in 1 BOXGEL124
65585-378-02WhiskCare 375Fragrance Free208.2 L in 1 DRUMGEL208.24
65585-378-03WhiskCare 375Fragrance Free0.118 L in 1 BOTTLE, PLASTICGEL0.1184
65585-378-04WhiskCare 375Fragrance Free24 in 1 BOXGEL244
65585-378-04WhiskCare 375Fragrance Free0.118 L in 1 BOTTLE, PLASTICGEL0.1184
65585-378-05WhiskCare 375Fragrance Free0.237 L in 1 BOTTLE, PUMPGEL0.2374
65585-378-05WhiskCare 375Fragrance Free12 in 1 BOXGEL124
65585-378-06WhiskCare 375Fragrance Free8 in 1 BOXGEL84
65585-378-06WhiskCare 375Fragrance Free1 L in 1 BAGGEL14
65585-378-07WhiskCare 375Fragrance Free3.785 L in 1 BOTTLE, PLASTICGEL3.7854
65585-378-08WhiskCare 375Fragrance Free1 L in 1 BAGGEL14
65585-378-08WhiskCare 375Fragrance Free6 in 1 BOXGEL64

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
65585-378WHISKCARE 375 FRAGRANCE FREE (ALCOHOL) GEL [WHISK PRODUCTS, INC.]4Current NDC, Legacy NDC, 13 package rows20240727_c6787b12-ab90-4305-a6cc-55fd2c57cd2d.zip

Products#

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

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

NDC Codes#

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
WhiskCare 375 Fragrance FreeALCOHOLWhisk Products, Inc.c6787b12-ab90-4305-a6cc-55fd2c57cd2d2024-07-26WarningsExact identifier
ndc (package): 65585-378-01
ndc (package): 65585-378-04
ndc (package): 65585-378-08
ndc (package): 65585-378-02
ndc (package): 65585-378-06
ndc (package): 65585-378-07
ndc (package): 65585-378-05
ndc (package): 65585-378-03
ndc (product): 65585-378
ndc11 (package): 65585037804
ndc11 (package): 65585037807
ndc11 (package): 65585037802
ndc11 (package): 65585037808
ndc11 (package): 65585037805
ndc11 (package): 65585037806
ndc11 (package): 65585037801
ndc11 (package): 65585037803
spl id: 1e26bbb9-0c68-fb0f-e063-6294a90aa6a8
spl set id: c6787b12-ab90-4305-a6cc-55fd2c57cd2d

Reported adverse events (FAERS/openFDA)#

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