Antibacterial Hand Sanitizer
FDA Label NDC 78887-001

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Ankit Llc for the product Antibacterial Hand Sanitizer (NDC 78887-001). 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, uses, 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

Alcohol 75% v/v.

Purpose

Antiseptic

Uses

Eliminate bacteria and viral matter on the skin.

Warnings

Do not use

  • on children under 2 months of age
  • on open wounds

    • When using:

    Avoid contact with face. eyes. and broken skin. In case of eye contact, flush with clean water and seek medical assistance.

    Stop use and contact a doctor if:
    Irritation or redness occurs.

Otc - Keep Out Of Reach Of Children

Keep out of reach of children. In case of ingestion. seek medical help or contact a Poison Control Center immediately.

Directions

  • Dispense a liberal amount of product on hands, enough to coat palms and fingers and then rub until dry.
  • Supervise small children to ensure proper usage and prevent ingestion.

Other Information

  • Store below 110°F[43°C].
  • May discolor certain fabrics/surfaces.

Inactive Ingredients

Water, Aloe, Carbomer, Triethanolamine.

Package Label - Principal Display Panel

Label (Label1)

Label (Label1)

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