Sanimax
FDA Label NDC 79308-001

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Syndicate One Group Inc for the product Sanimax (NDC 79308-001). 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, use, 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

decreases bacteria on skin.

Warnings

For external use only.

Flammable. Keep away from heat and flame.

When using the product

  • keep out of eyes, in case of contact with eyes, flush thoroughly with water
  • avoid contact with broken skin
  • do not inhale or ingest
  • do not reuse wipe
  • do not flush in toilet

    • 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

  • Wipe down surface thoroughly and allow to air-dry.
  • For children under 6, use only under adult supervision
  • Not recommended for infants

Other Information

  • do not store above 105°F

Inactive Ingredients

purified water, glycerin. aloe barbadensis extract, phenoxyethanol, ethylhexlyglycerin, propylene glycol

* Please review the disclaimer below.