Shelter Point Sanitizer
FDA Label NDC 76601-101

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Shelter Point Distillery Corporation for the product Shelter Point Sanitizer (NDC 76601-101). 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 drug facts, active ingredient, purpose, uses, warnings, directions, other information, packaging, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Label Section Quick Index

Drug Facts

Active Ingredient

Ethyl alcohol 75%

Purpose

Antiseptic

Uses

  • hand sanitizer to decrease bacteria on the skin
  • recommended for repeated use
  • for use when soap and water are not available

Warnings

Flammable, keep away from fire/flame

For external use only

Do not use 

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

    • When using this product  •  do not get into eyes. In case of contact, rinse eyes thoroughly with water

    Stop use and ask a doctor if 

    • irritation and redness develop
    • condition persists more for more than 72 hours

Directions

  • wet hands thoroughly with product and allow to dry without wiping
  • supervise children 6 years of age when using this product to avoid swallowing

Other Information

  • store between 15-30°C (59-86°F)
  • avoid freezing and excessive heat above 40°C (104°F)
  • do not use if tamper seal is broken

Packaging

Image (Label03)

Image (Label03)

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