Daisy Dnd
FDA Label NDC 78951-002

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Daisy Nail Product Inc. for the product Daisy Dnd (NDC 78951-002). 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[s], warnings, otc - keep out of reach of children, directions, other information, inactive ingredients, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Label Section Quick Index

Active Ingredient

Ethyl Alcohol 75% v/v.

Purpose

Antiseptic

Use[S]

  • to decrease bacteria on the skin that could cause disease
  • recommended for repeated use

Warnings

For external use only- hands.
Flammable, keep away from heat or flame.
Do not use

  • in children less than 2 months of age
  • on open skin wounds

    • When using this product

    • keep out of eyes, in case of contact with eyes, rinse eyes thoroughly with water.
    • avoid contact with broken skin.
    • do not inhale or ingest.

      • Stop use and ask a doctor if skin irritation develops.

Otc - Keep Out Of Reach Of Children

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Directions

  • Wet hand thoroughly and allow to dry without wiping.
  • For children under 6, use only under adult supervision.
  • Not recommended for infants.

Other Information

  • Store between 20°C-25°C (68-77°F).
  • May discolor certain fabrics and surfaces.

Inactive Ingredients

Glycerin, Bitandiol, Carboxypolymethylene, Vitamin E.

Package Label - Principal Display Panel

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