Whiskcare 375 Gel
FDA Label NDC 65585-378

Full FDA labeling including Indications, Dosage, Usage, and Precautions

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Whisk Products, Inc. for the product Whiskcare 375 (NDC 65585-378). This document serves as the official prescribing information, containing essential scientific data and clinical materials required for healthcare providers and patients.

This specific version of the label includes detailed information regarding active ingredient, purpose, use, warnings, otc - keep out of reach of children, directions, inactive ingredients, package label.principal display panel, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Label Section Quick Index

Active Ingredient

Ethyl Alcohol 60% v/v

Purpose

Skin Sanitizer

Use

Hand sanitizer to help reduce amount of bacteria on the skin

Warnings

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.

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

Otc - Keep Out Of Reach Of Children

Keep out of reach of children.

Directions

  • 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

Water, Propylene Glycol, Carbomer, Glycerin, Triethanolamine

Package Label.Principal Display Panel

Product Label (Wc375 55)

Product Label (Wc375 55)

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